Hydrogen Sulfide and Cancer

Abstract

Recent studies revealed increased expression of various hydrogen sulfide (H₂S)-producing enzymes in cancer cells of various tissue types, and new roles of H₂S in the pathophysiology of cancer have emerged. This is particularly evident in cancers of the colon and ovaries, where the malignant cells both overexpress cystathionine-β-synthase (CBS) and produce increased amounts of H₂S, which enhances tumor growth and spread by (a) stimulating cellular bioenergetics, (b) activating proliferative, migratory, and invasive signaling pathways, and (c) enhancing tumor angiogenesis. Importantly, in preclinical models of these cancers, either pharmacological inhibition or genetic silencing of CBS was shown to be sufficient to suppress cancer cell bioenergetics in vitro, inhibit tumor growth and metastasis in vivo, and enhance the antitumor efficacy of frontline chemotherapeutic agents, providing a strong rationale for the development of CBS-targeted inhibitors as anticancer therapies. However, the observation that inhibition of H₂S biosynthesis exerts anticancer effects is contradicted by other studies showing that increasing H₂S with exogenous donors also exerts antitumor actions. Herein, we present a brief review of the scientific literature documenting the function of H₂S, H₂S donors, and transsulfuration enzymes in cancers from various tissue types, and propose that the paradoxical actions of H₂S can be resolved by considering the bell-shaped pharmacology of H₂S, whereby lower (endogenous) H₂S production tends to promote, while higher (generated from exogenously added H₂S donors) tends to inhibit cancer cell proliferation. Finally, we suggest areas for future investigations to expand our knowledge of this nascent field.