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p53 Mutations and c‐erbB‐2 Amplification in Intraductal and Invasive Breast Carcinomas of High Histologic Grade

机译:高组织学级别的导管内和浸润性乳腺癌中的p53突变和c-erbB-2扩增

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摘要

In order to clarify the clinical significance of mutations of the p53 gene and amplification of the c‐erbB‐2 gene in breast carcinoma, these gene alterations were examined in 101 invasive, seven predominantly intraductal and 10 intraductal breast carcinomas by single‐strand conformation polymorphism‐direct sequencing or Southern blot‐hybridization analysis. p53 mutations were detected in 32 (32%) of the invasive cases and two (12%) of the 17 intraductal/predominantly intraductal cases, whereas c‐erbB‐2 amplification was detected in 14 (14%) of the invasive and six (35%) of the intraductal/predominantly intraductal cases. Irrespective of differences in the positions and types of the mutations, cases carrying p53 mutations were almost always Grade 3 histologically and with a low hormone‐receptor value. Since p53 mutations as well as c‐erbB‐2 amplification were detected almost selectively in Grade 3 cases but were not associated with lymph nodal status in invasive breast cancer, these two gene alterations could be indicators of prognosis of disease independent of lymph nodal status. Even in intraductal/predominantly intraductal carcinoma, these gene alterations were almost always detected in tumors of higher histologic grade. Thus, it is suggested that these gene alterations occur in breast cancers showing a high proliferation rate irrespective of the presence of invasion, and that other molecular alterations are involved in the process of breast cancer invasion.
机译:为了阐明乳腺癌中p53基因突变和c-erbB-2基因扩增的临床意义,通过单链构象多态性对101例浸润性,7例主要为导管内和10例导管内乳腺癌中的这些基因改变进行了检查。直接测序或Southern blot杂交分析。在侵入性病例中有32例(32%)和17例导管内/主要是导管内病例中检测到p53突变,而在14例(14%)侵入性病例中检测到c-erbB-2扩增,六例( 35%)的导管内/导管内病例。不论突变的位置和类型如何,携带p53突变的病例在组织学上几乎都是3级,激素受体值低。由于在3级病例中几乎选择性地检测到p53突变以及c-erbB-2扩增,但与浸润性乳腺癌的淋巴结状态无关,因此这两个基因改变可能是独立于淋巴结状态的疾病预后指标。即使在导管内/主要是导管内癌中,也几乎总是在组织学等级较高的肿瘤中检测到这些基因改变。因此,建议这些基因改变发生在显示高增殖率的乳腺癌中,而与侵袭的存在无关,并且其他分子改变也参与了乳腺癌侵袭的过程。

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