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Relationship between alterations of p16~(INK4a) and p14~(ARF) genes of CDKN2A locus and gastric carcinogenesis

机译:CDKN2A基因座p16〜(INK4a)和p14〜(ARF)基因改变与胃癌发生的关系

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Objective To investigate the relationship between alterations of p16~(INK4a) and p14~(ARF) genes and gastric carcinogenesis. Methods The tumors and neighboring gastric tissues from 48 patients with gastric cancer were studied. The homozygous deletion, mutation, methylation of the CpG islands, and mRNA expression of p16~(INK4a) and p14~(ARF) genes were assessed by PCR, PCR-SSCP, PCR based methylation assay, and RT-PCR. Results ① The homozygous deletion rate of p16~(INK4a) and p14~(ARF) was 35.4% (17/48), and no homozygous deletion was examined in any gastric tissue neighboring the tumor. ② There was no point mutation of p16~(INK4a) and p14~(ARF) in 31 gastric cancers without homozygous deletion or in the matched gastric tissues adjacent to the tumor. ③ Methylation of the CpG islands of p16~(INK4a) and p14~(ARF) was detected in 47. 9% (23/48) of gastric cancers, while methylation was observed only in 2 of 48 gastric tissues neighboring the cancer with a significant difference (P<0. 01). ④ The loss rate of p16~(INK4a) mRNA was 47. 9% (23/48) in gastric cancer, and the patients of the combined methylation of exons 1α and 2 had a higher loss rate (100%, 6/6) of p16~(INK4a) mRNA than those of the methylation of the other exons (11. 8%, 2/17, P<0. 01) ; the loss rate of p14~(ARF) mRNA was 45. 8% (22/48) in gastric cancer, and patients with the combined methylation of exons 1β and 2 had a higher loss rate (100%, 3/3) of p14~(ARF) mRNA than those of the methylation of the other exons (15%, 3/20, P<0. 05). ⑤ The combined loss of p16~(INK4a) and p14~(ARF) mRNAs was examined in 1 (5. 6%) of 18 patients of well and moderately-differentiated carcinomas, and 11 (36.7%) of 30 patients of poorly and not-differentiated carcinomas with a significant difference (P<0. 05). Conclusion p16~(INK4a) and p14~(ARF) genes are frequently inactivated by homozygous deletion and methylation of the 5 ' CpG islands in gastric cancer, which may play an important role in the carcinogenesis of gastric cancer.
机译:目的探讨p16〜(INK4a)和p14〜(ARF)基因的变化与胃癌发生的关系。方法对48例胃癌患者的肿瘤及周围胃组织进行研究。通过PCR,PCR-SSCP,基于PCR的甲基化分析和RT-PCR评估CpG岛的纯合缺失,突变,甲基化以及p16〜(INK4a)和p14〜(ARF)基因的mRNA表达。结果①p16〜(INK4a)和p14〜(ARF)的纯合缺失率为35.4%(17/48),在肿瘤附近的任何胃组织中均未检测到纯合缺失。 ②31例无纯合缺失的胃癌或癌旁癌旁胃组织中,p16〜(INK4a)和p14〜(ARF)均无点突变。 ③在47. 9%(23/48)的胃癌中检测到p16〜(INK4a)和p14〜(ARF)的CpG岛甲基化,而在癌旁的48个胃组织中只有2个甲基化。显着差异(P <0。01)。 ④胃癌中p16〜(INK4a)mRNA的丢失率为47. 9%(23/48),外显子1α和2联合甲基化的患者丢失率更高(100%,6/6) p16〜(INK4a)mRNA的表达比其他外显子甲基化的表达高(11. 8%,2/17,P <0。01);胃癌中p14〜(ARF)mRNA的丢失率为45. 8%(22/48),外显子1β和2甲基化的甲基化患者的p14丢失率更高(100%,3/3) 〜(ARF)mRNA高于其他外显子的甲基化(15%,3/20,P <0。05)。 ⑤在18例高分化和中分化癌患者中,有1例(5. 6%)检测了p16〜(INK4a)和p14〜(ARF)mRNA的联合损失,对30例中度和弱度癌患者,检测了11例(36.7%)。未分化癌有显着性差异(P <0。05)。结论p16〜(INK4a)和p14〜(ARF)基因经常被5'CpG岛的纯合缺失和甲基化所灭活,这可能在胃癌的发生中起重要作用。

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