General Commentary ARTICLE
Commentary: Fasting-Mimicking Diet Reduces HO-1 to Promote T Cell-Mediated Tumor Cytotoxicity
- 1Department of Biomedical and Biotechnological Sciences, University of Catania, Catania, Italy
- 2Center for Translational Medicine (CTM), International Clinical Research Center (ICRC), St. Anne’s University Hospital, Brno, Czechia
A commentary on
Fasting-Mimicking Diet Reduces HO-1 to Promote T Cell-Mediated Tumor Cytotoxicity
by Di Biase S, Lee C, Brandhorst S, Manes B, Buono R, Cheng CW, et al. Cancer Cell (2016) 30:136–46. doi: 10.1016/j.ccell.2016.06.005
Heme oxygenase (HO)-1 is an evolutionarily conserved enzyme expressed in mammalian cells. This protein is the first and rate-limiting enzyme in heme catabolism, degrading heme to equimolar quantities of carbon monoxide (CO), free iron, and biliverdin; biliverdin later converts to bilirubin, while free iron is directly sequestered by ferritin (1). HO-1 is expressed at low levels under basal conditions, and it is induced by polyphenols and a variety of stimuli such as inflammation, oxidative stress, hyperoxia, and hypoxia (2). Such upregulation represents an intrinsic defense mechanism to maintain cellular homeostasis. In cancer cells, HO-1 is considered to play a major role as an essential survival factor, protecting against chemotherapy-induced reactive oxygen species increase. In particular, exposure to CO sensitized prostate cancer cells but not normal cells to chemotherapy (3). Similarly, CO treatment results in positive alterations of tumor microenvironment impeding lung cancer growth through the modulation of macrophages (4). Interestingly, recent findings showed that other mechanisms not related to HO-1 enzymatic activity might be responsible for its antitumor and chemoresistance activities (5, 6). In particular, HO-1 nuclear translocation has been shown mediating, at least in part, some of these activities (7). Surprisingly, so far such non-enzymatic effects in cancer cells were only described for tumors of epithelial origin and some hematological malignancies. We read with great interest the elegant work of Di Biase et al. (8) in which the authors showed that fasting-mimicking diet (FMD) significantly reduced HO-1 expression in cancer cells (i.e., breast cancer and melanoma), whereas it increased the protein levels in normal cells. The authors further showed that this effect resulted in a significant increase in the number of cytotoxic CD8+ tumor-infiltrating lymphocytes. Such conclusions are based on the authors’ data showing that induction of HO-1 by pharmacological mean (i.e., hemin) or gene overexpression abolished the beneficial effect of FMD mediated HO-1 reduction on chemosensitivity. Interestingly, the authors stated in their manuscript that such external manipulation of HO-1 resulted only in a partial abolishment of the STS effects. In this respect, we would like to highlight authors’ data (Figure S5E) showing abundant HO-1 protein exclusively in the nuclear fraction in untreated control cells, and no signal at all upon STS, meaning that expression rather than nuclear translocation is affected. These data do suggest that nuclear HO-1 strongly, if not totally, contributes to 4T1 cells fitness, and may lead to the hypothesis that hemin may have a role not only in HO-1 upregulation and activation but also on its nuclear import. Consistently with this observation, previous published data demonstrated that hemin, a strong inducer of HO-1 expression and HO activity, can induce nuclear translocation of HO-1 in two different prostate cancer cells (9). Conversely, the authors also showed that HO-1 inhibitor ZnPP sensitized breast cancer cells (4T1) to cyclophosphamide under normal conditions in vitro (Figure 4G). It should be taken into due account that ZnPP is not a specific inhibitor of HO-1 activity since it results also in a significant inhibition of the constitutive isoform (i.e., HO-2) activity (10). In addition, ZnPP induce a significant increase of HO-1 protein expression due to intracellular heme overload, thus providing more substrate for the cleavage necessary for nuclear compartmentalization. Finally, this work further demonstrates the need of appropriate molecular tools to dissect the enzymatic function of HO-1 from its non-canonical functions.
GV, RA, and MV contributed to critical review of the literature and wrote the manuscript.
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.
This work was supported by the European Social Fund and European Regional Development Fund—Project MAGNET (No. CZ.02.1.01/0.0/0.0/15_003/0000492) to MV.
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3. Wegiel B, Gallo D, Csizmadia E, Harris C, Belcher J, Vercellotti GM, et al. Carbon monoxide expedites metabolic exhaustion to inhibit tumor growth. Cancer Res (2013) 73:7009–21. doi:10.1158/0008-5472.CAN-13-1075
4. Nemeth Z, Csizmadia E, Vikstrom L, Li M, Bisht K, Feizi A, et al. Alterations of tumor microenvironment by carbon monoxide impedes lung cancer growth. Oncotarget (2016) 7(17):23919–32. doi:10.18632/oncotarget.8081
5. Tibullo D, Barbagallo I, Giallongo C, La Cava P, Parrinello N, Vanella L, et al. Nuclear translocation of heme oxygenase-1 confers resistance to imatinib in chronic myeloid leukemia cells. Curr Pharm Des (2013) 19:2765–70. doi:10.2174/1381612811319150012
6. Tibullo D, Barbagallo I, Giallongo C, Vanella L, Conticello C, Romano A, et al. Heme oxygenase-1 nuclear translocation regulates bortezomibinduced cytotoxicity and mediates genomic instability in myeloma cells. Oncotarget (2016) 7(20):28868–80. doi:10.18632/oncotarget.7563
8. Di Biase S, Lee C, Brandhorst S, Manes B, Buono R, Cheng CW, et al. Fasting-mimicking diet reduces HO-1 to promote T cell-mediated tumor cytotoxicity. Cancer Cell (2016) 30:136–46. doi:10.1016/j.ccell.2016.06.005
Keywords: fasting, chemotherapy, liver neoplasms, nuclear localization, chemoresistance
Citation: Li Volti G, Avola R and Vinciguerra M (2017) Commentary: Fasting-Mimicking Diet Reduces HO-1 to Promote T Cell-Mediated Tumor Cytotoxicity. Front. Oncol. 7:116. doi: 10.3389/fonc.2017.00116
Received: 21 December 2016; Accepted: 19 May 2017;
Published: 02 June 2017
Edited by:Ala-Eddin Al Moustafa, Qatar University, Qatar
Copyright: © 2017 Li Volti, Avola and Vinciguerra. 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: Giovanni Li Volti, firstname.lastname@example.org