Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, 7006 Trondheim, Norway.
Department of Pathology, St. Olav's Hospital, Trondheim University Hospital, 7006 Trondheim, Norway.
Int J Mol Sci. 2020 Aug 11;21(16):5751. doi: 10.3390/ijms21165751.
Cancers are believed to originate from stem cells. Previously, the hypothesis was that tumors developed due to dedifferentiation of mature cells. We studied the regulation of gastric acid secretion and showed that gastrin through the gastrin receptor stimulates enterochromaffin-like (ECL) cell histamine release and proliferation. In animal and human studies, we and others showed that long-term hypergastrinemia results in ECL cell-derived tumor through a sequence of hyperplasia, dysplasia, neuroendocrine tumors (NETs), and possibly neuroendocrine carcinomas (NECs) and adenocarcinomas of diffuse type. Perhaps, other cancers may also have their origin in differentiated cells. Knowledge of the growth regulation of the cell of origin is important in cancer prophylaxis and treatment. Physiology plays a central role in carcinogenesis through hormones and other growth factors. Every cell division implies a small risk of mutation; thus mitogens are also mutagens. Moreover, metastasis of slow proliferating cells may also explain so-called tumor dormancy and late recurrence.
癌症被认为起源于干细胞。以前,假设肿瘤是由于成熟细胞的去分化而发展的。我们研究了胃酸分泌的调节,发现胃泌素通过胃泌素受体刺激肠嗜铬样(ECL)细胞组胺释放和增殖。在动物和人体研究中,我们和其他人表明,长期高胃泌素血症会导致 ECL 细胞衍生的肿瘤,通过一系列的增生、发育不良、神经内分泌肿瘤(NET),可能还有神经内分泌癌(NEC)和弥漫型腺癌。也许,其他癌症也可能起源于分化细胞。了解起始细胞的生长调控对癌症的预防和治疗很重要。生理学通过激素和其他生长因子在致癌作用中起着核心作用。每次细胞分裂都意味着发生突变的小风险;因此有丝分裂原也是诱变剂。此外,缓慢增殖细胞的转移也可以解释所谓的肿瘤休眠和晚期复发。