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中国乳腺癌患者表皮生长因子受体(EGFR)关键信号通路基因的突变分析

Mutational analysis of key EGFR pathway genes in Chinese breast cancer patients.

作者信息

Tong Lin, Yang Xue-Xi, Liu Min-Feng, Yao Guang-Yu, Dong Jian-Yu, Ye Chang-Sheng, Li Ming

机构信息

School of Biotechnology, Breast Center Nanfang Hospital, Southern Medical University, Guangzhou, China.

出版信息

Asian Pac J Cancer Prev. 2012;13(11):5599-603. doi: 10.7314/apjcp.2012.13.11.5599.

Abstract

BACKGROUND

The epidermal growth factor receptor (EGFR) is a potential therapeutic target for breast cancer; however, its use does not lead to a marked clinical response. Studies of non-small cell lung cancer and colorectal cancer showed that mutations of genes in the PIK3CA/AKT and RAS/RAF/MEK pathways, two major signalling cascades downstream of EGFR, might predict resistance to EGFR-targeted agents. Therefore, we examined the frequencies of mutations in these key EGFR pathway genes in Chinese breast cancer patients.

METHODS

We used a high-throughput mass-spectrometric based cancer gene mutation profiling platform to detect 22 mutations of the PIK3CA, AKT1, BRAF, EGFR, HRAS, and KRAS genes in 120 Chinese women with breast cancer.

RESULTS

Thirteen mutations were detected in 12 (10%) of the samples, all of which were invasive ductal carcinomas (two stage I, six stage II, three stage III, and one stage IV). These included one mutation (0.83%) in the EGFR gene (rs121913445-rs121913432), three (2.5%) in the KRAS gene (rs121913530, rs112445441), and nine (7.5%) in the PIK3CA gene (rs121913273, rs104886003, and rs121913279). No mutations were found in the AKT1, BRAF, and HRAS genes. Six (27.3%) of the 22 genotyping assays caused mutations in at least one sample and three (50%) of the six assays queried were found to be mutated more than once.

CONCLUSIONS

Mutations in the EGFR pathway occurred in a small fraction of Chinese breast cancers. However, therapeutics targeting these potential predictive markers should be investigated in depth, especially in Oriental populations.

摘要

背景

表皮生长因子受体(EGFR)是乳腺癌潜在的治疗靶点;然而,使用针对它的治疗方法并未带来显著的临床反应。对非小细胞肺癌和结直肠癌的研究表明,EGFR下游的两条主要信号级联途径PIK3CA/AKT和RAS/RAF/MEK途径中的基因突变可能预示着对EGFR靶向药物的耐药性。因此,我们检测了中国乳腺癌患者中这些关键EGFR途径基因的突变频率。

方法

我们使用基于高通量质谱的癌症基因突变分析平台,检测120名中国乳腺癌女性患者的PIK3CA、AKT1、BRAF、EGFR、HRAS和KRAS基因的22种突变。

结果

在12个(10%)样本中检测到13种突变,所有这些样本均为浸润性导管癌(2例I期、6例II期、3例III期和1例IV期)。其中包括EGFR基因中的1种突变(0.83%,rs121913445 - rs121913432)、KRAS基因中的3种突变(2.5%,rs121913530,rs112445441)以及PIK3CA基因中的9种突变(7.5%,rs121913273,rs104886003和rs121913279)。在AKT1、BRAF和HRAS基因中未发现突变。22种基因分型检测中有6种(27.3%)在至少一个样本中导致突变,所检测的6种检测中有3种(50%)被发现发生多次突变。

结论

EGFR途径中的突变在中国乳腺癌患者中占比很小。然而,针对这些潜在预测标志物的治疗方法应进行深入研究,尤其是在东方人群中。

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