Hypothesis and Theory ARTICLE
Two distinct etiologies of gastric cardia adenocarcinoma: interactions among pH, Helicobacter pylori, and bile acids
- Division of Molecular Diagnostic Pathology, Department of Pathology, Shiga University of Medical Science, Otsu, Shiga, Japan
Gastric cancer can be classified as cardia and non-cardia subtypes according to the anatomic site. Although the gastric cancer incidence has decreased steadily in several countries over the past 50 years, the incidence of cardia cancers and esophageal adenocarcinoma (EAC) continue to increase. The etiological factors involved in the development of both cardia cancers and EACs are associated with high animal fat intake, which causes severe obesity. Central obesity plays roles in cardiac-type mucosa lengthening and partial hiatus hernia development. There are two distinct etiologies of cardia cancer subtypes: one associated with gastroesophageal reflux (GER), which predominantly occurs in patients without Helicobacter pylori (H. pylori) infection and resembles EAC, and the other associated with H. pylori atrophic gastritis, which resembles non-cardia cancer. The former can be developed in the environment of high volume duodenal content reflux, including bile acids and a higher acid production in H. pylori–negative patients. N-nitroso compounds, which are generated from the refluxate that includes a large volume of bile acids and are stabilized in the stomach (which has high levels of gastric acid), play a pivotal role in this carcinogenesis. The latter can be associated with the changing colonization of H. pylori from the distal to the proximal stomach with atrophic gastritis because a high concentration of soluble bile acids in an environment of low acid production is likely to act as a bactericide or chemorepellent for H. pylori in the distal stomach. The manuscript introduces new insights in causative factors of adenocarcinoma of the cardia about the role of bile acids in gastro-esophageal refluxate based upon robust evidences supporting interactions among pH, H. pylori, and bile acids.
Gastric cancer is the sixth most common type of cancer and the fourth most common cause of cancer-related deaths worldwide (Ferlay et al., 2013). Gastric cancer can be classified according to the anatomic site as cardia (the upper part of the stomach adjoining the esophagus) and non-cardia (the mid and distal stomach) subtypes. Although the incidence of gastric cancer has steadily declined in several countries over the past 50 years, the overall decline is opposite to the subsite-specific increase in cardia cancers (Chow et al., 1998b; Carr et al., 2013). The increase in incidence is approximately seven fold, a more substantial increase than that in several other malignancies (Carr et al., 2013). Potential differences in the presentation and outcome of patients with gastric cardia or non-cardia adenocarcinoma may exist (Shi et al., 2011). Although it has been reported that cardia cancers may be related to gastroesophageal reflux (GER) similar to esophageal adenocarcinoma (EAC), the etiology of adenocarcinoma of the cardia remains unclear and controversial (Ye et al., 2001).
It is widely accepted that chronic mucosal inflammation causes the majority of gastric cancers due to Helicobacter pylori (H. pylori) infection (International Agency for Research on Cancer, 1994). However, the roles of H. pylori infection in the development of cardia cancer are contradictory (Chow et al., 1998a; Eslick et al., 1999; Ekstrom et al., 2001; Helicobacter and Cancer Collaborative Group, 2001; Limburg et al., 2001; Kamangar et al., 2006, 2007). Several studies indicate two distinct etiologies of cardia cancer: one that is more commonly associated with GER in H. pylori–negative than in H. pylori–positive patients and resembles EAC; and the other that is associated with H. pylori atrophic gastritis and resembles non-cardia cancer (McColl, 2006; Hansen et al., 2007; Derakhshan et al., 2008). In this manuscript, we try to explain the potential mechanisms involved in the development of gastric cardia adenocarcinoma with two distinct etiologies by elucidating the interaction among pH, H. pylori, and bile acids.
Cardia Adenocarcinoma Associated with GER Resembling EAC
Here we attempt to explain the possible mechanism involved in the development of cardia adenocarcinoma associated with GER by considering the causative factors of EAC.
Gastroesophageal Reflux Disease and Barrett Esophagus: Major Risk Factors for EAC
Most cases of esophageal cancer arise as squamous cell carcinoma or adenocarcinoma. Forty years ago, approximately 75% of diagnosed esophageal cancer cases, even those in the United States (U.S.), were esophageal squamous cell carcinoma and the remaining 25% were EAC. Among Caucasian men, the incidence of EAC has increased since the mid-1970s, and EAC has become the leading type of esophageal cancer, representing 80% of cases (Devesa et al., 1998; Enzinger and Mayer, 2003; Absi et al., 2013).
Gastroesophageal reflux disease (GERD) and Barrett esophagus are major risk factors for EAC, the risk for which increases with the frequency and duration of reflux symptoms (Lagergren et al., 1999; Wu et al., 2003; Anandasabapathy et al., 2007). Frequent reflux of the gastric juices, which contain acid, pepsin, and bile, is thought to induce Barrett esophagus, a condition of columnar metaplasia of the esophageal squamous epithelium damaged by GER (Souza et al., 2002; Theisen et al., 2005; Spechler and Souza, 2014). U.S. gastroenterology societies require esophageal biopsies to show intestinal metaplasia with goblet cells for the definitive diagnosis of Barrett esophagus (Wang and Sampliner, 2008; Spechler et al., 2011; ASGE Standards of Practice Committee et al., 2012). It has been widely accepted that an intestinal-type mucosa is the precursor of EAC (Ruol et al., 2000). However, it has been recently accepted that a cardiac-type mucosa without the intestinal goblet cells background of EAC is also occasionally encountered (Takubo et al., 2005, 2009; Kushima et al., 2013).
Roles of Central Obesity in Cardiac-type Mucosa Lengthening and Partial Hiatus Hernia Development
Abdominal obesity promotes GERD by elevating intra-abdominal pressure, which produces a hiatus hernia (El-Serag, 2008). Studies comparing computed tomography–measured abdominal fat composition showed that a large amount of visceral abdominal fat relative to subcutaneous fat is associated with a significant increase in the risk of Barrett esophagus (El-Serag et al., 2014). A recent study of 24 healthy H. pylori–negative volunteers with a small waist circumference and 27 with a large waist circumference reported that central obesity is associated with the intrasphincteric extension of gastric acid, allowing it to move proximally within the intrasphincteric reflux, and cardiac-type mucosal lengthening, which predisposes subjects to cardia adenocarcinoma (Robertson et al., 2013). Furthermore, according to a recent study of healthy volunteers without a history of GERD, central obesity and the use of a waist belt can produce a partial hiatus hernia and contribute to excess acid exposure of the distal esophageal mucosa, leading to metaplastic columnar changes (Lee et al., 2014).
Role of High Animal Fat Intake in EAC Development
A high fat intake, which can be a cause of central obesity, plays a role in an increased risk of GERD symptoms and erosive esophagitis, which are risk factors for EAC (El-Serag et al., 2005). The mechanism underlying this effect remains unclear; however, it may be proven by the increasing rates of GERD in the U.S. because the fat content of its food supply has increased by 38% between 1909 and 1988 (Raper et al., 1992). To examine the roles of high animal fat intake in the etiology of EAC, we fed a high animal fat diet to rats with reflux of the duodenal contents (Chen et al., 2007). First, Wistar rats in the control group were fed a low soybean oil diet and the other rats in the high-fat group were fed a high cow fat diet. The resulting morphological changes between these groups were then evaluated up to 30 weeks after surgery. The rats with reflux of the duodenal contents in the high-fat group showed a significantly higher incidence of Barrett esophagus and Barrett dysplasia than those in the control group. In addition, the incidence of EAC in the high-fat group was also slightly higher than that in the control group (Chen et al., 2007). These findings suggest that a high animal fat intake plays a pivotal role in EAC. In the clinical setting, it has been reported that high-fat dairy is associated with an increased risk of EAC (Navarro Silvera et al., 2008).
High Dietary Animal Fat Changes the Bile Acid Composition
We compared the total level and composition of bile acids in the bile juice collected from the common bile ducts of rats that had not undergone surgery (Chen et al., 2007). The bile juice was aspirated after the animals had been fed different diets for 1 month, and the bile acid concentrations were measured. High dietary animal fat changed the bile acid composition and increased the concentration of taurine conjugates in the bile juice (Chen et al., 2007). The chemical characteristics of bile in humans are governed by the pKa of the individual bile acids. Free bile acids have a pKa of approximately 7 and comprise approximately 2% of the bile. Glycine-conjugated bile acids have a pKa of 4.3–5.2 and comprise >60% of the bile, while taurine-conjugated bile acids have a pKa of 1.8–1.9 and comprise 20% of the bile, resulting in a ratio of glycine to taurine conjugates of approximately 3:1 (Nair and Kritchenvski, 1971; Stamp, 2002). Because only taurine conjugates are soluble among various bile acids in humans with intact gastric acid production and can affect the epithelium, an increase in taurine-conjugated bile acids in the refluxate under acidic conditions may play a role in Barrett carcinogenesis and cancer progression.
In a study examining bile acid, the esophageal samples taken from 10 asymptomatic subjects and 30 patients with GERD symptoms were analyzed using modified high-performance liquid chromatography (Nehra et al., 1999). There was a significantly greater proportion of secondary bile acids, deoxycholic acids, and taurodeoxycholic acids in patients with erosive esophagitis and Barrett esophagus/stricture. Taurocholic acid was also significantly increased in the Barrett esophagus/stricture group compared with the minimal injury group (Nehra et al., 1999). The study concluded that mixed reflux is more harmful than acid reflux alone and that possible toxic synergism exists between the taurine conjugates and the acid (Nehra et al., 1999). These findings are consistent with those of our animal experiments mentioned above.
Endogenous DNA Adducts and N-nitroso Bile acids
To explore the causative factors of EAC, thiazolidine-4-carboxylic acid (thioproline) was administered as a nitrite scavenger to rats considered the gastroduodenal contents reflux model (Kumagai et al., 2004). Postoperatively, we divided the reflux animals into two diet groups. Animals in the control group were given a normal diet, while the thioproline group was given food containing 0.5% thioproline. All esophageal sections in both groups were histologically evaluated. EAC developed in 38.9% of the control group, whereas no EAC was detected in the thioproline group (Fisher exact test, P < 0.05). We then proposed that nitroso compounds derived from duodenal contents reflux play a crucial role in the development of EAC (Kumagai et al., 2004). We also performed a similar experiment using the rat duodenal contents reflux model for gastric carcinogenesis. This study also suggested a connection between nitroso compounds and gastric carcinogenesis (Suo et al., 2006). Furthermore, Terasaki et al. (2008) detected the endogenous DNA adducts produced from N-nitroso bile acid conjugates, such as N-nitrosoglycocholic acid and N-nitrosotaurocholic acid, in the glandular stomach of the duodenal contents reflux rats. These observations confirmed that N-nitrosotaurocholic acid and N-nitrosoglycocholic acid are formed by the nitrosation of glycocholic acid and taurocholic acid, respectively. These studies suggest that nitrosated bile acid conjugates, which have mutagenicity, could contribute to the development of both EAC and gastric carcinogenesis.
Highly Acidic Condition Stabilizes Mutagenic N-nitroso Bile Acids
The pathogenesis of GERD is multifactorial since it involves transient lower esophageal sphincter relaxation as well as other lower esophageal sphincter pressure abnormalities (Castell et al., 2004). GERD is a complex problem caused by many factors that are exacerbated when the patient is in the supine position (Castell et al., 2004). Gastric contents are easily pooled, and N-nitroso compounds could be generated at night, in the gastric juice with the refluxate including bile acids in the fornix located on the posterior side of the body. Moreover, both the esophagus and the proximal cardia portion are easily exposed to the N-nitroso compounds by transient lower esophageal sphincter relaxation as well as other lower esophageal sphincter pressure abnormalities in the supine position (Macke et al., 2011). We reported that one of these nitroso compounds, N-nitroso glycocholic, rapidly decomposed under alkaline conditions (pH 9) [t(1/2) = 0.96 h] but remained quite stable under acidic (pH 2) [t(1/2) = 12.8 h] and neutral (pH 7) [t(1/2) = 7.8 h] conditions (Araki et al., 2008). These findings suggest that a highly acidic condition also contributes to carcinogenesis as a stabilizer of N-nitroso bile acids.
H. pylori Protects Against GERD
There are inverse associations between the presence of H. pylori (particularly cagA+ strains) and disorders such as GERD, Barrett esophagus, and EAC (Vicari et al., 1998; Peek et al., 1999; Vaezi et al., 2000; Ye et al., 2004; Islami and Kamangar, 2008), suggesting a protective role of H. pylori. One potential mechanism for this effect could be that H. pylori colonization diminishes gastric acidity; therefore, during reflux episodes, the highly acidic refluxate in H. pylori–negative patients may be more damaging to the esophageal epithelium than the low acidic refluxate from the stomach with H. pylori–associated atrophic gastritis.
Cardia Adenocarcinoma Associated with H. pylori Atrophic Gastritis Resembling Non-cardia Cancer
Here we attempt to explain the possible mechanism of the development of cardia adenocarcinoma resembling non-cardia cancer by considering the interactions among pH, H. pylori, and bile acids.
Relationship between H. pylori and Non-cardia Gastric Carcinogenesis
H. pylori generally colonizes to the pyloric antrum and H. pylori was designated a class I carcinogen by the World Health Organization (International Agency for Research on Cancer, 1994). Thus, the best-established risk factor for non-cardia gastric cancer is H. pylori infection (Kamangar et al., 2006; Brenner et al., 2009). However, H. pylori infection is required for gastric cancer to develop but not for gastric carcinogenesis. There are several animal models of H. pylori–induced carcinogenesis, but unless the bacteria are combined with a chemical carcinogen or hypergastrinemia, none of these models reliably produce a malignancy similar to that observed in humans (Hagiwara et al., 2011; Hayakawa et al., 2013; Tsukamoto et al., 2013; Yu et al., 2014; Graham, 2015). H. pylori has been shown to promote the production of inflammatory mediators such as interleukin-1β and tumor necrosis factor-α, potent suppressors of stomach juice secretion. The increase in stomach pH may lead to the spread of H. pylori from the antrum to the corpus, resulting in enhanced inflammation in the mucosa of the corpus followed by parietal cell destruction and irreversible hypochlorhydria (Takashima et al., 2001; Peek and Blaser, 2002).
Cardia Adenocarcinoma Associated with H. pylori Atrophic Gastritis
Although most studies of Western populations found no association or an inverse association, few studies of Asian populations have found a positive association between H. pylori seropositivity and cardia cancer (Helicobacter and Cancer Collaborative Group, 2001; Dawsey et al., 2002). Recently, two studies reported on the origin of gastroesophageal junction adenocarcinoma or esophagogastric junction, which are similar meaning to cardia adenocarcinoma. Horii et al. reported that the two distinct types of cancer of different origin might be mixed in cardia adenocarcinoma: Barrett esophageal cancer might be associated with high gastric acid secretion and reflux of gastric acid into the esophagus, and cancer resembling distal gastric cancer might be associated with gastric atrophy and low gastric acid secretion (Horii et al., 2011). Yamada et al. reported that approximately half of patients with cardia adenocarcinoma harbor histological gastritis (Yamada et al., 2014). These findings suggest that a part of cardia adenocarcinoma can be associated with H. pylori atrophic gastritis resembling non-cardia cancer in especially Asian countries.
Interactions Among Bile Acids, pH, and H. pylori
Mechanism of Duodenal Ulcer Treatment by Antisecretory Therapy
The combination of a high duodenal acid load and H. pylori infection is possibly a critical event in the pathogenesis of H. pylori–related duodenal ulcer disease (Graham and Osato, 2000). Graham et al. suggested that, because glycine-conjugated bile acids are precipitated at an acidic pH, H. pylori can survive in gastric metaplasia and any event that leads to an increase in the duodenal acid load predisposes patients with H. pylori infection to duodenal ulcer diseases (Graham et al., 1996). They and other authors also reported that any condition that reduces the duodenal acid load (e.g., antisecretory therapy) allows the bile acids to remain in the solution, inhibits the growth of H. pylori, and promotes ulcer healing (Han et al., 1996; Graham and Osato, 2000).
Long-term use of Proton Pump Inhibitors Exacerbates Corpus Atrophic Gastritis in H. pylori–positive Patients
H. pylori predominantly colonizes the gastric antrum in subjects in whom acid production is intact. In contrast, in subjects in whom acid production is decreased by whatever mechanism, including the use of proton pump inhibitors (PPIs), H. pylori colonizes the body of the stomach (Kuipers, 2006). Although there is no proof that the PPI use increases the risk of gastric cancer at present, PPI therapy affects the pattern and severity of H. pylori gastritis and accelerates the process of corpus gland loss (Kuipers, 2006). We recently proposed the mechanism of how the long-term use of PPIs exacerbates corpus atrophic gastritis in H. pylori–positive patients with GERD that includes interactions among bile acids, pH, and H. pylori (Mukaisho et al., 2014; Hagiwara et al., 2015). The original idea about the mechanism of duodenal ulcer treatment by antisecretory therapy was proposed in the papers mentioned above.
Duodenogastric reflux including bile reportedly occurs even in healthy individuals (Keane et al., 1981; Sonnenberg et al., 1982; Thompson, 1982; Heading, 1983; Muller-Lissner et al., 1983), and bile reflux is increased in patients with GERD (Kauer et al., 1997). Bile acids are significant chemorepellents for the bacillus H. pylori (Worku et al., 2004). PPIs administration inhibits gastric acid production and changes the concentration of soluble bile acids in the stomach. Because taurine conjugates have a pKa of 1.8–1.9 and glycine conjugates have a pKa of 4.3–5.2, only taurine conjugates are soluble in an acidic environment. However, glycine conjugates as well as taurine conjugates become soluble in the presence of PPIs administration. Because the concentration of soluble bile acids in patients with GERD on PPI therapy is considerably higher than that in normal subjects with intact acid production, especially in the distal stomach with duodenogastric reflux including bile, the colonization of H. pylori changes the pattern from antral-predominant to corpus-predominant (Mukaisho et al., 2014).
Mechanism of Changing Colonization of H. pylori in Atrophic Gastritis
The similar phenomena may occur in the stomach with H. pylori–associated atrophic gastritis because this condition induces an environment of low acid production in the stomach. The high concentration of soluble bile acids in the environment of low acid production, especially in the distal stomach, is likely to act as a bactericide or chemorepellent for H. pylori. In contrast, the concentration of soluble bile acids in the proximal stomach is less than that of distal stomach. H. pylori may then colonize within the proximal rather than distal stomach.
Furthermore, it has been reported that the development of atrophic gastritis late in life diminishes or eliminates H. pylori colonization (Karnes et al., 1991). Potential reasons for the specific association of H. pylori with a normal gastric mucosal epithelium include a low pH requirement for metabolic processes; dependence on specific nutrients, mucins, or cell-surface components that are specific features of the gastric epithelium; or the inability to compete in environments in which other microbes are more abundant. These findings also might explain the phenomenon of the changing colonization of H. pylori from the distal to the proximal stomach.
Based on anatomic site, gastric cancer can be classified as cardia or non-cardia subtypes. There are two distinct etiologies of cardia cancer: one associated with GER and resembles EAC, and the other associated with H. pylori atrophic gastritis and resembles non-cardia cancer. The former can develop in the environment of high volume duodenal contents reflux, which includes bile acids and a higher acid production in H. pylori–negative than in H. pylori–positive patients. The latter can develop because of the changing colonization of H. pylori from the distal to the proximal stomach with atrophic gastritis in patients with H. pylori infection. Although the reason for the striking increase in the proportion of cases of cardia cancer as well as EAC remains unknown, it may at least partially be explained by increasing rates of GERD, which induces duodenal contents reflux into the stomach.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Absi, A., Adelstein, D. J., and Rice, T. (2013). Esophageal Cancer. Available at: http://www.clevelandclinicmeded.com/medicalpubs/diseasemanagement/hematologyoncology/esophageal-cancer/
Anandasabapathy, S., Jhamb, J., Davila, M., Wei, C., Morris, J., and Bresalier, R. (2007). Clinical and endoscopic factors predict higher pathologic grades of Barrett dysplasia. Cancer 109, 668–674. doi: 10.1002/cncr.22451
ASGE Standards of Practice Committee, Evans, J. A., Early, D. S., Fukami, N., Ben-Menachem, T., Chandrasekhara, V., et al. (2012). The role of endoscopy in Barrett’s esophagus and other premalignant conditions of the esophagus. Gastrointest. Endosc. 76, 1087–1094. doi: 10.1016/j.gie.2012.08.004
Carr, J. S., Zafar, S. F., Saba, N., Khuri, F. R., and El-Rayes, B. F. (2013). Risk factors for rising incidence of esophageal and gastric cardia adenocarcinoma. J. Gastrointest. Cancer 44, 143–151. doi: 10.1007/s12029-013-9480-z
Castell, D. O., Murray, J. A., Tutuian, R., Orlando, R. C., and Arnold, R. (2004). Review article: the pathophysiology of gastro-oesophageal reflux disease—oesophageal manifestations. Aliment. Pharmacol. Ther. 20(Suppl. 9), 14–25. doi: 10.1111/j.1365-2036.2004.02238.x
Chen, K. H., Mukaisho, K., Sugihara, H., Araki, Y., Yamamoto, G., and Hattori, T. (2007). High animal-fat intake changes the bile-acid composition of bile juice and enhances the development of Barrett’s esophagus and esophageal adenocarcinoma in a rat duodenal-contents reflux model. Cancer Sci. 98, 1683–1688. doi: 10.1111/j.1349-7006.2007.00605.x
Chow, W. H., Blaser, M. J., Blot, W. J., Gammon, M. D., Vaughan, T. L., Risch, H. A., et al. (1998a). An inverse relation between cagA+ strains of Helicobacter pylori infection and risk of esophageal and gastric cardia adenocarcinoma. Cancer Res. 58, 588–590.
Chow, W. H., Blot, W. J., Vaughan, T. L., Risch, H. A., Gammon, M. D., Stanford, J. L., et al. (1998b). Body mass index and risk of adenocarcinomas of the esophagus and gastric cardia. J. Natl. Cancer Inst. 90, 150–155. doi: 10.1093/jnci/90.2.150
Derakhshan, M. H., Malekzadeh, R., Watabe, H., Yazdanbod, A., Fyfe, V., Kazemi, A., et al. (2008). Combination of gastric atrophy, reflux symptoms and histological subtype indicates two distinct aetiologies of gastric cardia cancer. Gut 57, 298–305. doi: 10.1136/gut.2007.137364
Devesa, S. S., Blot, W. J., and Fraumeni, J. F. Jr. (1998). Changing patterns in the incidence of esophageal and gastric carcinoma in the United States. Cancer 83, 2049–2053. doi: 10.1002/(SICI)1097-0142(19981115)83:10<2049::AID-CNCR1>3.0.CO;2-2
Ekstrom, A. M., Held, M., Hansson, L. E., Engstrand, L., and Nyrén, O. (2001). Helicobacter pylori in gastric cancer established by CagA immunoblot as a marker of past infection. Gastroenterology 121, 784–791. doi: 10.1053/gast.2001.27999
El-Serag, H. B., Hashmi, A., Garcia, J., Richardson, P., Alsarraj, A., Fitzgerald, S., et al. (2014). Visceral abdominal obesity measured by CT scan is associated with an increased risk of Barrett’s oesophagus: a case-control study. Gut 63, 220–229. doi: 10.1136/gutjnl-2012-304189
El-Serag, H. B., Satia, J. A., and Rabeneck, L. (2005). Dietary intake and the risk of gastro-oesophageal reflux disease: a cross sectional study in volunteers. Gut 54, 11–17. doi: 10.1136/gut.2004.040337
Eslick, G. D., Lim, L. L., Byles, J. E., Xia, H. H., and Talley, N. J. (1999). Association of Helicobacter pylori infection with gastric carcinoma: a meta-analysis. Am. J. Gastroenterol. 94, 2373–2379. doi: 10.1111/j.1572-0241.1999.01360.x
Ferlay, J., Soerjomataram, I., Ervik, M., Dikshit, R., Eser, S., Mathers, C., et al. (2013). Cancer Incidence and Mortality Worldwide: IARC CancerBase No. 11. GLOBOCAN 2012 v1.0. Lyon: International Agency for Research on Cancer. Available at: http://globocan.iarc.fr
Graham, D. Y., Genta, R. M., Go, M. F., and Malarty, H. (1996). “Which is the most important factor in duodenal ulcer pathogenesis: the strain of Helicobacter pylori or the host?” in Helicobacter pylori: Basic Mechanisms to Clinical Cure, eds R. H. Hunt and G. N. J. Tytgat (Lancaster: Kluwer Academic Publishers), 85–91.
Graham, D. Y., and Osato, M. S. (2000). H. pylori in the pathogenesis of duodenal ulcer: interaction between duodenal acid load, bile, and H. pylori. Am. J. Gastroenterol. 95, 87–91. doi: 10.1111/j.1572-0241.2000.01704.x
Hagiwara, T., Mukaisho, K., Nakayama, T., Hattori, T., and Sugihara, H. (2015). Proton pump inhibitors and helicobacter pylori-associated pathogenesis. Asian Pac. J. Cancer Prev. 16, 1315–1319. doi: 10.7314/APJCP.2015.16.4.1315
Hagiwara, T., Mukaisho, K., Nakayama, T., Sugihara, H., and Hattori, T. (2011). Long-term proton pump inhibitor administration worsens atrophic corpus gastritis and promotes adenocarcinoma development in Mongolian gerbils infected with Helicobacter pylori. Gut 60, 624–630. doi: 10.1136/gut.2010.207662
Hansen, S., Vollset, S. E., Derakhshan, M. H., Fyfe, V., Melby, K. K., Aase, S., et al. (2007). Two distinct aetiologies of cardia cancer; evidence from premorbid serological markers of gastric atrophy and Helicobacter pylori status. Gut 56, 918–925. doi: 10.1136/gut.2006.114504
Helicobacter and Cancer Collaborative Group. (2001). Gastric cancer and Helicobacter pylori: a combined analysis of 12 case control studies nested within prospective cohorts. Gut 49, 347–353. doi: 10.1136/gut.49.3.347
Horii, T., Koike, T., Abe, Y., Kikuchi, R., Unakami, H., Iijima, K., et al. (2011). Two distinct types of cancer of different origin may be mixed in gastroesophageal junction adenocarcinomas in Japan: evidence from direct evaluation of gastric acid secretion. Scand. J. Gastroenterol. 46, 710–719. doi: 10.3109/00365521.2011.565069
Kamangar, F., Dawsey, S. M., Blaser, M. J., Perez-Perez, G. I., Pietinen, P., Newschaffer, C. J., et al. (2006). Opposing risks of gastric cardia and non cardia gastric adenocarcinomas associated with Helicobacter pylori seropositivity. J. Natl. Cancer Inst. 98, 1445–1452. doi: 10.1093/jnci/djj393
Kamangar, F., Qiao, Y. L., Blaser, M. J., Sun, X. D., Katki, H., Fan, J. H., et al. (2007). Helicobacter pylori and esophageal and gastric cancers in a prospective study in China. Br. J. Cancer 96, 172–176. doi: 10.1038/sj.bjc.6603517
Karnes, W. E. Jr., Samloff, I. M., Siurala, M., Kekki, M., Sipponen, P., Kim, S. W., et al. (1991). Positive serum antibody and negative tissue staining for Helicobacter pylori in subjects with atrophic body gastritis. Gastroenterology 101, 167–174.
Kauer, W. K., Peters, J. H., DeMeester, T. R., Feussner, H., Ireland, A. P., Stein, H. J., et al. (1997). Composition and concentration of bile acid reflux into the esophagus of patients with gastroesophageal reflux disease. Surgery 122, 874–881. doi: 10.1016/S0039-6060(97)90327-5
Keane, F. B., Dimagno, E. P., and Malagelada, J. R. (1981). Duodenogastric reflux in humans: its relationship to fasting antroduodenal motility and gastric, pancreatic, and biliary secretion. Gastroenterology 81, 726–731.
Kumagai, H., Mukaisho, K., Sugihara, H., Miwa, K., Yamamoto, G., and Hattori, T. (2004). Thioproline inhibits development of esophageal adenocarcinoma induced by gastroduodenal reflux in rats. Carcinogenesis 25, 723–727. doi: 10.1093/carcin/bgh067
Kushima, R., Mukaisho, K. I., Takemura, S., Sugihara, H., Hattori, T., and Vieth, M. (2013). Barrett’s esophagus: analyses from human and experimental animal studies. Pathologe 34, 138–147. doi: 10.1007/s00292-012-1731-4
Lagergren, J., Bergström, R., Lindgren, A., and Nyrén O. (1999). Symptomatic gastroesophageal reflux as a risk factor for esophageal adenocarcinoma. N. Engl. J. Med. 340, 825–831. doi: 10.1056/NEJM199903183401101
Lee, Y. Y., Wirz, A. A., Whiting, J. G., Robertson, E. V., Smith, D., Weir, A., et al. (2014). Waist belt and central obesity cause partial hiatus hernia and short-segment acid reflux in asymptomatic volunteers. Gut 63, 1053–1060. doi: 10.1136/gutjnl-2013-305803
Limburg, P., Qiao, Y., Mark, S., Wang, G., Perez-Perez, G., Blaser, M., et al. (2001). Helicobacter pylori seropositivity and subsite- specific gastric cancer risks in Linxian, China. J. Natl. Cancer Inst. 93, 226–233. doi: 10.1093/jnci/93.3.226
Macke, R. A., Nason, K. S., Mukaisho, K., Hattori, T., Fujimura, T., Sasaki, S., et al. (2011). Barrett’s esophagus and animal models. Ann. N. Y. Acad. Sci. 1232, 392–400. doi: 10.1111/j.1749-6632.2011.06061.x
Mukaisho, K., Hagiwara, T., Nakayama, T., Hattori, T., and Sugihara, H. (2014). Potential mechanism of corpus-predominant gastritis after PPI therapy in Helicobacter pylori-positive patients with GERD. World J. Gastroenterol. 20, 11962–11965. doi: 10.3748/wjg.v20.i34.11962
Muller-Lissner, S. A., Fimmel, C. J., Sonnenberg, A., Will, N., Müller-Duysing, W., Heinzel, F., et al. (1983). Novel approach to quantify duodenogastric reflux in healthy volunteers and in patients with type I gastric ulcer. Gut 24, 510–518. doi: 10.1136/gut.24.6.510
Navarro Silvera, S. A., Mayne, S. T., Risch, H., Gammon, M. D., Vaughan, T. L., Chow, W. H., et al. (2008). Food group intake and risk of subtypes of esophageal and gastric cancer. Int. J. Cancer. 123, 852–860. doi: 10.1002/ijc.23544
Nehra, D., Howell, P., Williams, C. P., Pye, J. K., and Beynon, J. (1999). Toxic bile acids in gastro-oesophageal reflux disease: influence of gastric acidity. Gut 44, 598–602. doi: 10.1136/gut.44.5.598
Peek, R. M. Jr., Vaezi, M. F., Falk, G. W., Goldblum, J. R., Perez-Perez, G. I., Richter, J. E., et al. (1999). Role of Helicobacter pylori cagA+ strains and specific host immune responses on the development of premalignant and malignant lesions in the gastric cardia. Int. J. Cancer. 82, 520–524. doi: 10.1002/(SICI)1097-0215(19990812)82:4<520::AID-IJC9>3.0.CO;2-7
Robertson, E. V., Derakhshan, M. H., Wirz, A. A., Lee, Y. Y., Seenan, J. P., Ballantyne, S. A., et al. (2013). Central obesity in asymptomatic volunteers is associated with increased intrasphincteric acid reflux and lengthening of the cardiac mucosa. Gastroenterology 145, 730–739. doi: 10.1053/j.gastro.2013.06.038
Ruol, A., Parenti, A., Zaninotto, G., Merigliano, S., Costantini, M., Cagol, M., et al. (2000). Intestinal metaplasia is the probable common precursor of adenocarcinoma in Barrett esophagus and adenocarcinoma of the gastric cardia. Cancer 88, 2520–2528. doi: 10.1002/1097-0142(20000601)88:11<2520::AID-CNCR13>3.0.CO;2-L
Shi, Y., Hu, Z., Wu, C., Dai, J., Li, H., Dong, J., et al. (2011). A genome-wide association study identifies new susceptibility loci for non-cardia gastric cancer at 3q13.31 and 5p13.1. Nat. Genet. 43, 1215–1218. doi: 10.1038/ng.978
Souza, R. F., Shewmake, K., Terada, L. S., and Spechler, S. J. (2002). Acid exposure activates the mitogen-activated protein kinase pathways in Barrett’s oesophagus. Gastroenterology 122, 299–307. doi: 10.1053/gast.2002.30993
Spechler, S. J., Sharma, P., Souza, R. F., Inadomi, J. M., and Shaheen, N. J. (2011). American Gastroenterological Association technical review on the management of Barrett’s esophagus. Gastroenterology 140, e18–e52. doi: 10.1053/j.gastro.2011.01.031
Stamp, D. H. (2002). Three hypotheses linking bile to carcinogenesis in the gastrointestinal tract: certain bile salts have properties that may be used to complement chemotherapy. Med. Hypotheses. 59, 398–405. doi: 10.1016/S0306-9877(02)00125-1
Suo, M., Mukaisho, K., Shimomura, A., Sugihara, H., and Hattori, T. (2006). Thioproline prevents carcinogenesis in the remnant stomach induced by duodenal reflux. Cancer Lett. 237, 256–262. doi: 10.1016/j.canlet.2005.06.019
Takashima, M., Furuta, T., Hanai, H., Sugimura, H., and Kaneko, E. (2001). Effects of Helicobacter pylori infection on gastric acid secretion and serum gastrin levels in Mongolian gerbils. Gut 48, 765–773. doi: 10.1136/gut.48.6.765
Takubo, K., Aida, J., Naomoto, Y., Sawabe, M., Arai, T., Shiraishi, H., et al. (2009). Cardiac rather than intestinal-type background in endoscopic resection specimens of minute Barrett adenocarcinoma. Hum. Pathol. 40, 65–74. doi: 10.1016/j.humpath.2008.06.008
Takubo, K., Vieth, M., Aryal, G., Honma, N., Sawabe, M., Arai, T., et al. (2005). Islands of squamous epithelium and their surrounding mucosa in columnar-lined esophagus: a pathognomonic feature of Barrett’s esophagus? Hum. Pathol. 36, 269–274. doi: 10.1016/j.humpath.2005.01.012
Terasaki, M., Totsuka, Y., Nishimura, K., Mukaisho, K., Chen, K. H., Hattori, T., et al. (2008). Detection of endogenous DNA adducts, O-carboxymethyl-2′-deoxyguanosine and 3-ethanesulfonic acid-2′-deoxycytidine, in the rat stomach after duodenal reflux. Cancer Sci. 99, 1741–1746. doi: 10.1111/j.1349-7006.2008.00871.x
Theisen, J., Peters, J. H., Fein, M., Hughes, M., Hagen, J. A., Demeester, S. R., et al. (2005). The mutagenic potential of duodenoesophageal reflux. Ann. Surg. 241, 63–68. doi: 10.1097/01.sla.0000150072.55037.e3
Tsukamoto, T., Toyoda, T., Mizoshita, T., and Tatematsu, M. (2013). Helicobacter pylori infection and gastric carcinogenesis in rodent models. Semin. Immunopathol. 35, 177–190. doi: 10.1007/s00281-012-0357-1
Vaezi, M. F., Falk, G. W., Peek, R. M., Vicari, J. J., Goldblum, J. R., Perez-Perez, G. I., et al. (2000). CagA-positive strains of Helicobacter pylori may protect against Barrett’s esophagus. Am. J. Gastroenterol. 95, 2206–2211. doi: 10.1111/j.1572-0241.2000.02305.x
Vicari, J. J., Peek, R. M., Falk, G. W., Goldblum, J. R., Easley, K. A., Schnell, J., et al. (1998). The seroprevalence of cagA-positive Helicobacter pylori strains in the spectrum of gastroesophageal reflux disease. Gastroenterology 115, 50–57. doi: 10.1016/S0016-5085(98)70364-6
Wang, K. K., and Sampliner, R. E. (2008). Updated guidelines 2008 for the diagnosis, surveillance and therapy of Barrett’s esophagus. Am. J. Gastroenterol. 103, 788–797. doi: 10.1111/j.1572-0241.2008.01835.x
Yamada, M., Kushima, R., Oda, I., Mojtahed, K., Nonaka, S., Suzuki, H., et al. (2014). Different histological status of gastritis in superficial adenocarcinoma of the esophagogastric junction. Jpn. J. Clin. Oncol. 44, 65–71. doi: 10.1093/jjco/hyt167
Ye, W., Chow, W. H., Lagergren, J., Yin, L., and Nyrén, O. (2001). Risk of adenocarcinomas of the esophagus and gastric cardia in patients with gastroesophageal reflux diseases and after antireflux surgery. Gastroenterology 121, 1286–1293. doi: 10.1053/gast.2001.29569
Ye, W., Held, M., Lagergren, J., Engstrand, L., Blot, W. J., McLaughlin, J. K., et al. (2004). Helicobacter pylori infection and gastric atrophy: risk of adenocarcinoma and squamous-cell carcinoma of the esophagus and adenocarcinoma of the gastric cardia. J. Natl. Cancer Inst. 96, 388–396. doi: 10.1093/jnci/djh057
Keywords: Helicobacter pylori, cardia gastric adenocarcinoma, gastroesophageal reflux disease, bile acids, pH, atrophic gastritis
Citation: Mukaisho K, Nakayama T, Hagiwara T, Hattori T and Sugihara H (2015) Two distinct etiologies of gastric cardia adenocarcinoma: interactions among pH, Helicobacter pylori, and bile acids. Front. Microbiol. 6:412. doi: 10.3389/fmicb.2015.00412
Received: 31 January 2015; Accepted: 20 April 2015;
Published: 11 May 2015.
Edited by:Yeong Yeh Lee, Universiti Sains Malaysia, Malaysia
Reviewed by:Mohammad H. Derakhshan, University of Glasgow, UK
Askin Erdogan, Georgia Regents University, USA
Copyright © 2015 Mukaisho, Nakayama, Hagiwara, Hattori and Sugihara. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Ken-ichi Mukaisho, Division of Molecular Diagnostic Pathology, Department of Pathology, Shiga University of Medical Science, Seta-tsukinowa-cho, Otsu, Shiga 520-2192, Japan, email@example.com