Roschke Anna V, Lababidi Samir, Tonon Giovanni, Gehlhaus Kristen S, Bussey Kimberly, Weinstein John N, Kirsch Ilan R
Genetics Branch and Laboratory of Molecular Pharmacology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Proc Natl Acad Sci U S A. 2005 Feb 22;102(8):2964-9. doi: 10.1073/pnas.0405578102. Epub 2005 Feb 9.
Cancer is a genetic disease caused by genomic instability. In many cancers, this instability is manifested by chromosomal reconfigurations and karyotypic complexity. These features are particular hallmarks of the epithelial cancers that are some of the malignancies most resistant to long term control by current chemotherapeutic agents. We have asked whether we could use karyotypic complexity and instability as determinants for the screening of potential anticancer compounds. Using a panel of well characterized cancer cell lines, we have been able to identify specific groups of chemical compounds that are more cytotoxic toward the relatively more karyotypically complex and unstable panel members. Thus, we delineate an approach for the identification of "lead compounds" for anticancer drug discovery complementary to those that are focused at the outset on a given gene or pathway.
癌症是一种由基因组不稳定引起的遗传性疾病。在许多癌症中,这种不稳定性表现为染色体重排和核型复杂性。这些特征是上皮性癌的特殊标志,上皮性癌是目前化疗药物最难长期控制的恶性肿瘤之一。我们曾探讨是否可以将核型复杂性和不稳定性作为筛选潜在抗癌化合物的决定因素。通过使用一组特征明确的癌细胞系,我们已经能够鉴定出特定的化合物组,这些化合物对核型相对更复杂和不稳定的细胞系成员具有更强的细胞毒性。因此,我们描绘了一种用于鉴定抗癌药物研发“先导化合物”的方法,该方法与那些一开始就聚焦于特定基因或途径的方法互为补充。