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葡萄糖转运蛋白1(GLUT1)基因是结直肠癌患者潜在的缺氧标志物。

GLUT1 gene is a potential hypoxic marker in colorectal cancer patients.

作者信息

Chung Fu-Yen, Huang Ming-Yii, Yeh Ching-Sheng, Chang Hui-Jen, Cheng Tian-Lu, Yen Li-Chen, Wang Jaw-Yuan, Lin Shiu-Ru

机构信息

Graduate Institute of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan, Republic of China.

出版信息

BMC Cancer. 2009 Jul 20;9:241. doi: 10.1186/1471-2407-9-241.

Abstract

BACKGROUND

Tumor hypoxia is an important factor related to tumor resistance to radiotherapy and chemotherapy. This study investigated molecules synthesized in colorectal cancer cells during hypoxia to explore the possibility of developing molecular probes capable of detecting cell death and/or the efficiency of radiotherapy and chemotherapy.

METHODS

At first, we incubated two human colorectal adenocarcinoma cell lines SW480 (UICC stage II) and SW620 (UICC stage III) cells in hypoxic (< or =2% O2, 93% N2, and 5% CO2) and normoxic conditions (20% O2, 75% N2, and 5% CO2) for 24 h and 48 h. The relative expression ratio of GLUT1 mRNA in hypoxic conditions was analyzed by RT-PCR. Ten cancerous tissues collected from human colorectal cancer patients were examined. HIF-1alpha and HIF-2alpha levels were measured to indicate the degree of hypoxia, and gene expression under hypoxic conditions was determined. As a comparison, HIF-1alpha, HIF-2alpha, and GLUT1 levels were measured in the peripheral blood of 100 CRC patients.

RESULTS

Hypoxia-induced lactate was found to be elevated 3.24- to 3.36-fold in SW480 cells, and 3.06- to 3.17-fold in SW620 cells. The increased relative expression ratio of GLUT1 mRNA, under hypoxic conditions was higher in SW620 cells (1.39- to 1.72-fold elevation) than in SW480 cells (1.24- to 1.66-fold elevation). HIF-1alpha and HIF-2alpha levels were elevated and GLUT1 genes were significantly overexpressed in CRC tissue specimens. The elevated ratio of GLUT1 was higher in stage III and IV CRC tissue specimens than in the stage I and II (2.97-4.73 versus 1.44-2.11). GLUT1 mRNA was also increased in the peripheral blood of stage II and III CRC patients as compared to stage I patients, suggesting that GLUT1 may serve as a hypoxic indicator in CRC patients.

CONCLUSION

In conclusion, this study demonstrated that GLUT1 has the potential to be employed as a molecular marker to indicate the degree of hypoxia experienced by tumors circulating in the blood of cancer patients.

摘要

背景

肿瘤缺氧是与肿瘤对放疗和化疗耐药相关的一个重要因素。本研究调查了结肠癌细胞在缺氧状态下合成的分子,以探索开发能够检测细胞死亡和/或放疗及化疗效果的分子探针的可能性。

方法

首先,我们将两个人结肠腺癌细胞系SW480(国际抗癌联盟II期)和SW620(国际抗癌联盟III期)细胞分别置于缺氧(≤2%氧气、93%氮气和5%二氧化碳)和常氧条件(20%氧气、75%氮气和5%二氧化碳)下培养24小时和48小时。通过逆转录聚合酶链反应分析缺氧条件下葡萄糖转运蛋白1(GLUT1)信使核糖核酸的相对表达率。检测了从人类结肠癌患者收集的10个癌组织。测量缺氧诱导因子-1α(HIF-1α)和缺氧诱导因子-2α(HIF-2α)水平以指示缺氧程度,并确定缺氧条件下的基因表达。作为对照,测量了100例结直肠癌患者外周血中的HIF-1α、HIF-2α和GLUT1水平。

结果

发现缺氧诱导的乳酸在SW480细胞中升高3.24至3.36倍,在SW620细胞中升高3.06至3.17倍。缺氧条件下,SW620细胞中GLUT1信使核糖核酸相对表达率的升高(升高1.39至1.72倍)高于SW480细胞(升高1.24至1.66倍)。在结直肠癌组织标本中,HIF-1α和HIF-2α水平升高,GLUT1基因显著过表达。III期和IV期结直肠癌组织标本中GLUT1的升高比例高于I期和II期(2.97 - 4.73对1.44 - 2.11)。与I期患者相比,II期和III期结直肠癌患者外周血中的GLUT1信使核糖核酸也增加,这表明GLUT1可能作为结直肠癌患者的缺氧指标。

结论

总之,本研究表明GLUT1有潜力作为一种分子标志物,以指示癌症患者血液中循环肿瘤所经历的缺氧程度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3661/3087329/e244150c247a/1471-2407-9-241-1.jpg

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