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PIK3CA and TP53 Gene Mutations in Human Breast Cancer Tumors Frequently Detected by Ion Torrent DNA Sequencing

机译:离子激流DNA测序经常检测人乳腺癌肿瘤中的PIK3CA和TP53基因突变。

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摘要

Breast cancer is the most common malignancy and the leading cause of cancer deaths in women worldwide. While specific genetic mutations have been linked to 5–10% of breast cancer cases, other environmental and epigenetic factors influence the development and progression of the cancer. Since unique mutations patterns have been observed in individual cancer samples, identification and characterization of the distinctive breast cancer molecular profile is needed to develop more effective target therapies. Until recently, identifying genetic cancer mutations via personalized DNA sequencing was impractical and expensive. The recent technological advancements in next-generation DNA sequencing, such as the semiconductor-based Ion Torrent sequencing platform, has made DNA sequencing cost and time effective with more reliable results. Using the Ion Torrent Ampliseq Cancer Panel, we sequenced 737 loci from 45 cancer-related genes to identify genetic mutations in 105 human breast cancer samples. The sequencing analysis revealed missense mutations in PIK3CA, and TP53 genes in the breast cancer samples of various histologic types. Thus, this study demonstrates the necessity of sequencing individual human cancers in order to develop personalized drugs or combination therapies to effectively target individual, breast cancer-specific mutations.
机译:乳腺癌是全世界女性中最常见的恶性肿瘤,也是导致癌症死亡的主要原因。虽然特定的基因突变已与5-10%的乳腺癌病例相关,但其他环境和表观遗传因素也会影响癌症的发生和发展。由于已经在单个癌症样品中观察到独特的突变模式,因此需要鉴定和表征独特的乳腺癌分子谱以开发更有效的靶标疗法。直到最近,通过个性化的DNA测序鉴定遗传癌症突变是不切实际且昂贵的。下一代DNA测序的最新技术进步,例如基于半导体的Ion Torrent测序平台,使DNA测序的成本和时间更加有效,结果更加可靠。使用离子激增扩增小组,我们从45个与癌症相关的基因中测序了737个基因座,以鉴定105个人类乳腺癌样本中的基因突变。测序分析揭示了各种组织学类型的乳腺癌样本中PIK3CA和TP53基因的错义突变。因此,这项研究表明对人类癌症进行测序的必要性,以便开发出可有效靶向个体乳腺癌特异性突变的个性化药物或联合疗法。

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