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乳腺癌中6号染色体长臂杂合性缺失:可能存在四个缺失区域。

Loss of heterozygosity on the long arm of chromosome 6 in breast cancer: possibly four regions of deletion.

作者信息

Noviello C, Courjal F, Theillet C

机构信息

Institut de Génétique Moléculaire de Montpellier, UMR CNRS 9942, 1919 route de Mende, 34033 Montpellier Cedex 1, France.

出版信息

Clin Cancer Res. 1996 Sep;2(9):1601-6.

PMID:9816339
Abstract

Deletions and rearrangements involving chromosome 6q have been reported in a number of human cancers such as ovarian and breast tumors as well as melanoma and hemopoietic malignancies. To gain insight into the regions undergoing deletions on the long arm of chromosome 6, we performed a survey of loss of heterozygosity (LOH) at 11 CA repeat markers, mapping from 6q13 to 6q27 in 83 matched sets of tumor and blood DNAs from breast tumor patients. LOH was observed at all tested markers with frequencies ranging from 11.4 to 39.8% of the informative cases, whereas D2S123, a marker linked to the HMSH2 gene mapping in a region rarely presenting allele losses, showed 3.2%. LOH patterns were often complex, with a number of tumors presenting multiple interstitial losses, thus indicating that chromosome 6q can be severely rearranged in breast cancer. Patterns of losses and correlation between LOH occurring at adjacent markers suggested the existence of three (possibly four) distinct regions of allele losses. These were defined by: D6S251-D6S434 (6q13), D6S292-D6S310-D6S314-D6S311 (6q24-q25), and D6S441-D6S281 (6q27). The fourth and more hypothetical region was in the 6q21 region and defined by D6S287-D6S407. Interestingly, the region at 6q24-q25 defined by D6S292-D6S310-D6S314-D6S311 was predominantly observed in evolved and aggressive breast tumors. LOH at D6S314 was correlated with PR- tumors. All together, our data suggest the possible presence of several genes on 6q whose alteration may play a role in breast cancer formation and development.

摘要

据报道,在许多人类癌症中,如卵巢癌、乳腺癌、黑色素瘤和造血系统恶性肿瘤,都存在涉及6号染色体长臂的缺失和重排。为了深入了解6号染色体长臂上发生缺失的区域,我们对83例乳腺癌患者的肿瘤和血液DNA匹配样本进行了研究,检测了位于6q13至6q27区域的11个CA重复标记的杂合性缺失(LOH)情况。在所有检测的标记中均观察到了LOH,其频率在信息性病例的11.4%至39.8%之间,而与HMSH2基因连锁的标记D2S123位于一个很少出现等位基因缺失的区域,其LOH频率为3.2%。LOH模式通常很复杂,许多肿瘤呈现出多个间质缺失,这表明6号染色体长臂在乳腺癌中可能会发生严重重排。相邻标记处的缺失模式和LOH之间的相关性表明存在三个(可能四个)不同的等位基因缺失区域。这些区域分别由以下标记定义:D6S251 - D6S434(6q13)、D6S292 - D6S310 - D6S314 - D6S311(6q24 - q25)和D6S441 - D6S281(6q27)。第四个且更具推测性的区域位于6q21区域,由D6S287 - D6S407定义。有趣的是,由D6S292 - D6S310 - D6S314 - D6S311定义的6q24 - q25区域主要出现在进展期和侵袭性乳腺癌中。D6S314处的LOH与PR阴性肿瘤相关。总之,我们的数据表明6号染色体长臂上可能存在多个基因,其改变可能在乳腺癌的形成和发展中起作用。

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