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葡萄糖和胰岛素/胰岛素样生长因子对结肠癌细胞的调节作用。

Modifying Effects of Glucose and Insulin/Insulin-Like Growth Factors on Colon Cancer Cells.

作者信息

Berk Şeyda, Janssen Joseph A M J L, van Koetsveld Peter M, Dogan Fadime, Değerli Naci, Özcan Servet, Kelestimur Fahrettin, Hofland Leo J

机构信息

Department of Molecular Biology and Genetics, Faculty of Science, Sivas Cumhuriyet University, Sivas, Turkey.

Department of Internal Medicine, Division of Endocrinology, Erasmus Medical Center, Rotterdam, Netherlands.

出版信息

Front Oncol. 2021 Jul 5;11:645732. doi: 10.3389/fonc.2021.645732. eCollection 2021.

Abstract

There are only a few experimental studies which have investigated effects of glucose alone, and glucose in combination with insulin/insulin-like growth factors (IGF) on the growth of colon cancer. In the present study, we studied in human colorectal cancer cells originating from four Dukes' stages of colorectal cancer the effects of glucose, insulin and IGFs on proliferation, migration, cell cycle progression and gene expression of the IGF system. Growth of colon cancer cells originating from a Dukes' stage A was glucose-dependent, whereas growth of cancer cells from Dukes' stage B, C and D was glucose-independent. Stimulatory effects of insulin and IGFs on cell growth were observed only in colon cancer cells originating from Dukes' stage C and D. IGF-II stimulated migration in Dukes' stage B cells only. The growth stimulatory effects in Dukes' stage C and D colorectal cancer cells were accompanied by G2/M arrest and associated with an increased IGF-IR/IGF-II receptor ratio. In conclusion, our data suggest that the stimulating effects of glucose, IGFs and insulin on proliferation differ between colorectal cancer cells from early and late Dukes' stages. Stimulatory effects of glucose on proliferation appear predominantly present in stage Dukes' stage A colorectal cancer cells, while in contrast growth factor-mediated stimulation of cell proliferation is more pronounced in Dukes' late stage (metastasized) colorectal cancer cells. Moreover, our study suggests that a stringent glucose control may be important to control tumor growth in early stages of colorectal cancer, while inhibition of the endocrine actions of the IGFs and insulin become more important in the late (metastasized) stages of colorectal cancer to restrain growth of colon cancer cells.

摘要

仅有少数实验研究调查了单独葡萄糖以及葡萄糖与胰岛素/胰岛素样生长因子(IGF)联合使用对结肠癌生长的影响。在本研究中,我们在源自结直肠癌四个 Dukes 分期的人结肠癌细胞中,研究了葡萄糖、胰岛素和 IGF 对增殖、迁移、细胞周期进程以及 IGF 系统基因表达的影响。源自 Dukes A 期的结肠癌细胞生长依赖葡萄糖,而源自 Dukes B 期、C 期和 D 期的癌细胞生长不依赖葡萄糖。仅在源自 Dukes C 期和 D 期的结肠癌细胞中观察到胰岛素和 IGF 对细胞生长的刺激作用。IGF-II 仅刺激 Dukes B 期细胞的迁移。Dukes C 期和 D 期结直肠癌细胞中的生长刺激作用伴随着 G2/M 期阻滞,并与 IGF-IR/IGF-II 受体比例增加相关。总之,我们的数据表明,葡萄糖、IGF 和胰岛素对增殖的刺激作用在 Dukes 早期和晚期的结直肠癌细胞之间存在差异。葡萄糖对增殖的刺激作用主要出现在 Dukes A 期的结直肠癌细胞中,而相比之下,生长因子介导的细胞增殖刺激在 Dukes 晚期(转移)结直肠癌细胞中更为明显。此外,我们的研究表明,严格控制葡萄糖对于控制结直肠癌早期的肿瘤生长可能很重要,而在结直肠癌晚期(转移)抑制 IGF 和胰岛素的内分泌作用对于抑制结肠癌细胞生长变得更为重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd10/8287530/eaec9ad90538/fonc-11-645732-g001.jpg

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