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高血糖通过己糖胺生物合成途径加剧结肠癌的恶性程度。

Hyperglycemia exacerbates colon cancer malignancy through hexosamine biosynthetic pathway.

作者信息

Vasconcelos-Dos-Santos A, Loponte H F B R, Mantuano N R, Oliveira I A, de Paula I F, Teixeira L K, de-Freitas-Junior J C M, Gondim K C, Heise N, Mohana-Borges R, Morgado-Díaz J A, Dias W B, Todeschini A R

机构信息

Instituto de Biofísica Carlos Chagas Filho, Rio de Janeiro, Brazil.

Instituto de Bioquímica Médica Leopoldo de Meis, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.

出版信息

Oncogenesis. 2017 Mar 20;6(3):e306. doi: 10.1038/oncsis.2017.2.

Abstract

Hyperglycemia is a common feature of diabetes mellitus, considered as a risk factor for cancer. However, its direct effects in cancer cell behavior are relatively unexplored. Herein we show that high glucose concentration induces aberrant glycosylation, increased cell proliferation, invasion and tumor progression of colon cancer. By modulating the activity of the rate-limiting enzyme, glutamine-fructose-6-phosphate amidotransferase (GFAT), we demonstrate that hexosamine biosynthetic pathway (HBP) is involved in those processes. Biopsies from patients with colon carcinoma show increased levels of GFAT and consequently aberrant glycans' expression suggesting an increase of HBP flow in human colon cancer. All together, our results open the possibility that HBP links hyperglycemia, aberrant glycosylation and tumor malignancy, and suggest this pathway as a potential therapeutic target for colorectal cancer.

摘要

高血糖是糖尿病的常见特征,被认为是癌症的一个风险因素。然而,其对癌细胞行为的直接影响相对未被充分探索。在此我们表明,高葡萄糖浓度会诱导结肠癌的异常糖基化、细胞增殖增加、侵袭和肿瘤进展。通过调节限速酶谷氨酰胺 - 果糖 -6- 磷酸酰胺转移酶(GFAT)的活性,我们证明己糖胺生物合成途径(HBP)参与了这些过程。结肠癌患者的活检显示GFAT水平升高,进而异常聚糖表达增加,这表明人类结肠癌中HBP通量增加。总之,我们的结果揭示了HBP将高血糖、异常糖基化和肿瘤恶性联系起来的可能性,并表明该途径可能是结直肠癌的一个潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34fd/5533945/09dfb7e99f7b/oncsis20172f1.jpg

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