Department of Medicine, Division of Gastroenterology and Hepatology, Arizona Comprehensive Cancer Center, University of Arizona, Tucson, AZ 85724, USA.
Function (Oxf). 2021 Nov 26;3(1):zqab062. doi: 10.1093/function/zqab062. eCollection 2022.
Abetted by widespread usage of acid-suppressing proton pump inhibitors (PPIs), the mitogenic actions of the peptide hormone gastrin are being revisited as a recurring theme in various gastrointestinal (GI) malignancies. While pathological gastrin levels are intricately linked to hyperplasia of enterochromaffin-like cells leading to carcinoid development, the signaling effects exerted by gastrin on distinct cell types of the gastric mucosa are more nuanced. Indeed, mounting evidence suggests dichotomous roles for gastrin in both promoting and suppressing tumorigenesis. Here, we review the major upstream mediators of gastrin gene regulation, including inflammation secondary to infection and the use of PPIs. We further explore the molecular biology of gastrin in GI malignancies, with particular emphasis on the regulation of gastrin in neuroendocrine neoplasms. Finally, we highlight tissue-specific transcriptional targets as an avenue for targetable therapeutics.
在广泛使用抑制胃酸分泌的质子泵抑制剂(PPIs)的帮助下,作为各种胃肠道(GI)恶性肿瘤中反复出现的主题,胃泌素这种肽激素的促有丝分裂作用正在被重新审视。虽然病理性胃泌素水平与导致类癌发展的肠嗜铬样细胞增生密切相关,但胃泌素对胃黏膜不同细胞类型的信号作用更为微妙。事实上,越来越多的证据表明胃泌素在促进和抑制肿瘤发生方面具有双重作用。在这里,我们回顾了胃泌素基因调控的主要上游介质,包括感染引起的炎症和 PPI 的使用。我们进一步探讨了胃泌素在 GI 恶性肿瘤中的分子生物学,特别强调了胃泌素在神经内分泌肿瘤中的调节作用。最后,我们强调组织特异性转录靶标作为靶向治疗的途径。