Department of Oncology, Southwest Hospital, Third Military Medical University, 30 Gaotanyan Street, Shapingba District, Chongqing 400038, China.
J Cancer Res Clin Oncol. 2010 Nov;136(11):1697-707. doi: 10.1007/s00432-010-0828-5. Epub 2010 Mar 9.
Hypoxia in tumors is generally associated with chemoresistance and radioresistance. However, the correlation between the heterodimeric hypoxia-inducible factor-1 (HIF-1) and the multidrug resistance (MDR1) gene/transporter P-glycoprotein (P-gp) has not been clearly investigated. This study aims at examining the expression levels of HIF-1α and MDR1/P-gp in human colon carcinoma tissues and cell lines (HCT-116, HT-29, LoVo, and SW480) and ascertaining whether HIF-1α plays an important role in tumor multidrug resistance with MDR1/P-gp.
The expression and distribution of HIF-1α and P-gp proteins were detected in human colon carcinoma tissues and cell lines by immunohistochemistry and immunocytochemistry using streptavidin/peroxidase (SP) and double-label immunofluorescence methods. HIF-1α and MDR1 mRNA expression levels in cell lines were analyzed using RT-PCR under normoxic and hypoxic conditions, respectively.
The immunohistochemical method shows that HIF-1α and P-gp expression were not correlated with gender, age, location, and differentiation degree (P > 0.05). However, the expression of HIF-1α and P-gp at different Dukes' stages and whether involved in lymphatic invasion shows a significant difference (P < 0.05). Correlation analysis displays that HIF-1α protein expression was correlated significantly with P-gp expression (P < 0.01). Double-label immunofluorescence demonstrates that coexpression of HIF-1α and P-gp does exist in human colon carcinoma tissues. The mRNA expression of HIF-1α and MDR1 was detected in the four human colon carcinoma cell lines under both normoxia and hypoxia. Optical density values representing mRNA expression levels of HIF-1α and MDR1 were found to be significantly higher in the same type cells under hypoxic conditions than that under normoxic conditions, respectively (P < 0.01). However, no significant differences of HIF-1α or MDR1 mRNA expression were found among these cell lines, which exposed under the same PaO(2) cultural conditions (P > 0.05). And the immunocytochemistry results were corresponding with the analysis of mRNA expression.
These results suggest that hypoxia induce the expression of HIF-1α and MDR1/P-gp in colon carcinoma and HIF-1α expression may be associated with the gene MDR1 (P-gp) and interactively involved in the occurrence of tumor multidrug resistance.
肿瘤中的缺氧通常与化疗耐药和放疗耐药有关。然而,异二聚体缺氧诱导因子-1(HIF-1)与多药耐药(MDR1)基因/转运蛋白 P-糖蛋白(P-gp)之间的相关性尚未得到明确研究。本研究旨在检测人结肠癌组织和细胞系(HCT-116、HT-29、LoVo 和 SW480)中 HIF-1α和 MDR1/P-gp 的表达水平,并确定 HIF-1α是否在肿瘤多药耐药中与 MDR1/P-gp 发挥重要作用。
采用免疫组织化学和免疫细胞化学 SP 法和双标免疫荧光法检测人结肠癌组织和细胞系中 HIF-1α和 P-gp 蛋白的表达和分布。分别在常氧和缺氧条件下,通过 RT-PCR 分析细胞系中 HIF-1α和 MDR1mRNA 的表达水平。
免疫组化方法显示,HIF-1α和 P-gp 的表达与性别、年龄、部位和分化程度无关(P>0.05)。然而,不同 Dukes 分期的 HIF-1α和 P-gp 表达以及是否涉及淋巴浸润显示出显著差异(P<0.05)。相关性分析显示,HIF-1α蛋白表达与 P-gp 表达显著相关(P<0.01)。双标免疫荧光显示,HIF-1α和 P-gp 在人结肠癌组织中存在共表达。在常氧和缺氧条件下,检测了四种人结肠癌细胞系中 HIF-1α和 MDR1 的 mRNA 表达。在相同类型的细胞中,缺氧条件下 HIF-1α 和 MDR1mRNA 表达水平的光密度值明显高于常氧条件(P<0.01)。然而,在相同 PaO2 培养条件下,这些细胞系之间的 HIF-1α 或 MDR1mRNA 表达没有显著差异(P>0.05)。免疫细胞化学结果与 mRNA 表达分析结果相对应。
这些结果表明,缺氧诱导结肠癌中 HIF-1α和 MDR1/P-gp 的表达,HIF-1α 的表达可能与基因 MDR1(P-gp)相关,并与肿瘤多药耐药的发生相互作用。