同一患者组血液和癌症组织样本的细胞遗传学差异

O. Demirhan, D. Korkmaz
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摘要

乳腺癌(BC)是世界范围内女性最常见的恶性疾病。肿瘤组织中的基因组不稳定性与肿瘤进展有关。这些遗传变化可能有多种形式,包括数量和结构染色体异常(CAs)、表观遗传变化和基因表达改变。许多肿瘤组织是由遗传上不同的细胞群组成的,对这种异质性的原因和后果的研究在癌症研究中起着核心作用。本研究检测了散发性BC患者血液和癌组织中的CAs。我们的研究结果表明,BC组织中数字性别非整倍体的增加明显高于血液组织。癌症组织中这些非整倍体的增加似乎与癌症的发展和增加是相容的,并且可以在癌症的发病机制中发挥作用。这些变化与早期和长期接触致癌物,特别是雌激素一致。这些发现阐明了我们对乳腺组织中乳腺癌发生的认识,并促进了对女性乳腺癌风险评估和预防方法的改进。
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Cytogenetic differences in blood and cancer tissue samples of the same patient group
Breast cancer (BC) is the most prevalent malignant disease in females worldwide. Genomic instability in tumor tissue has been associated with tumor progression. These genetic changes may take a variety of forms, including numerical and structural chromosomal abnormalities (CAs), epigenetic changes, and gene expression alterations. Many tumor tissues are made up of genetically different cell populations, and the study of the causes and consequences of this heterogeneity play a central role in cancer research. In this study, CAs in blood and cancer tissues of patients with sporadic BC were examined. Our findings shows that the increase in numerical sex aneuploidy in BC tissues is significantly higher than in blood tissue. These aneuploidy increases in cancer tissues seem to be compatible with the development and increase of cancer, and can play a role in the pathogenesis of cancers. These changes are consistent with early and long-standing exposure to carcinogens, especially estrogens. These findings should clarify our understanding of breast carcinogenesis in breast tissues and promote development of improved methods for risk assessment and BC prevention in women.
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