Egawa C, Miyoshi Y, Taguchi T, Tamaki Y, Noguchi S
Department of Surgical Oncology, Osaka University Medical School, 2-2 E-10 Yamada-oka, Suita, Osaka 565-0871, Japan.
Jpn J Cancer Res. 2001 Jun;92(6):624-30. doi: 10.1111/j.1349-7006.2001.tb01140.x.
BRCA1 and BRCA2 mRNA expression in sporadic breast cancers was quantified by a real-time reverse transcriptase-polymerase chain reaction (RT-PCR), and the relationship of their expression with various clinicopathological factors was studied. BRCA2 mRNA levels (0.993 +/- 1.395, mean +/- SD (BRCA2 / beta-glucuronidase mRNA ratios)) were significantly (P < 0.01) higher than BRCA1 mRNA levels (0.519 +/- 0.570 (BRCA1 / beta-glucuronidase mRNA ratios)), and a weak but significant (r = 0.390, P < 0.01) correlation was observed between BRCA1 and BRCA2 mRNA expression levels. There was no significant association between BRCA1 mRNA expression and clinicopathological factors such as menstrual status, tumor size, lymph node status, estrogen and progesterone receptor status, and histological grade. On the other hand, there was a significant association between higher BRCA2 mRNA expression and estrogen receptor (ER) negativity (P < 0.01) or progesterone receptor (PR) negativity (P < 0.01) or high histological grade (P < 0.01). These results suggest a differential contribution of BRCA1 and BRCA2 in the pathogenesis of sporadic breast cancers. BRCA2 mRNA is speculated to be up-regulated in response to proliferation and genomic instability in high histological grade tumors.
通过实时逆转录聚合酶链反应(RT-PCR)对散发性乳腺癌中BRCA1和BRCA2 mRNA的表达进行定量,并研究其表达与各种临床病理因素的关系。BRCA2 mRNA水平(0.993±1.395,平均值±标准差(BRCA2/β-葡萄糖醛酸酶mRNA比值))显著高于BRCA1 mRNA水平(0.519±0.570(BRCA1/β-葡萄糖醛酸酶mRNA比值))(P<0.01),并且在BRCA1和BRCA2 mRNA表达水平之间观察到弱但显著的相关性(r = 0.390,P<0.01)。BRCA1 mRNA表达与月经状态、肿瘤大小、淋巴结状态、雌激素和孕激素受体状态以及组织学分级等临床病理因素之间无显著关联。另一方面,较高的BRCA2 mRNA表达与雌激素受体(ER)阴性(P<0.01)或孕激素受体(PR)阴性(P<0.01)或高组织学分级(P<0.01)之间存在显著关联。这些结果提示BRCA1和BRCA2在散发性乳腺癌发病机制中的作用存在差异。推测BRCA2 mRNA在高组织学分级肿瘤中因增殖和基因组不稳定而被上调。