Reversion of the ErbB malignant phenotype and the DNA damage response | |
Runkle, EA; Zhang, HT; Cai, Z; Zhu, ZG; Karger, BL; Wu, SL; O'Rourke, DM; Zhou, ZC; Wang, Q; Greene, MI | |
刊名 | EXPERIMENTAL AND MOLECULAR PATHOLOGY |
2012 | |
卷号 | 93期号:3页码:324-333 |
关键词 | HER ErbB EGFR DNA repair Double-strand breaks Ionizing radiation Nuclear compartmentalization SUN KASH LINC |
通讯作者 | Greene, MI (reprint author), Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA.,greene@reo.med.upenn.edu |
英文摘要 | The ErbB or HER family is a group of membrane bound tyrosine kinase receptors that initiate signal transduction cascades, which are critical to a wide range of biological processes. When over-expressed or mutated, members of this kinase family form homomeric or heteromeric kinase assemblies that are involved in certain human malignancies. Targeted therapy evolved from studies showing that monoclonal antibodies to the ectodomain of ErbB2/neu would reverse the malignant phenotype. Unfortunately, tumors develop resistance to targeted therapies even when coupled with genotoxic insults such as radiation. Radiation treatment predominantly induces double strand DNA breaks, which, if not repaired, are potentially lethal to the cell. Some tumors are resistant to radiation treatment because they effectively repair double strand breaks. We and others have shown that even in the presence of ionizing radiation, active ErbB kinase signaling apparently enhances the repair process, such that transformed cells resist genotoxic signal induced cell death. We review here the current understanding of ErbB signaling and DNA double strand break repair. Some studies have identified a mechanism by which DNA damage is coordinated to assemblies of proteins that associate with SUN domain containing proteins. These assemblies represent a new target for therapy of resistant tumor cells. (C) 2012 Elsevier Inc. All rights reserved. |
学科主题 | Pathology |
类目[WOS] | Pathology |
关键词[WOS] | DEPENDENT PROTEIN-KINASE ; EPIDERMAL-GROWTH-FACTOR ; DOUBLE-STRAND BREAK ; SQUAMOUS-CELL CARCINOMA ; SPINDLE POLE BODY ; XRCC4-DNA LIGASE-IV ; HUMAN TUMOR-CELLS ; PHASE-I/II TRIAL ; FACTOR RECEPTOR ; CATALYTIC SUBUNIT |
收录类别 | SCI |
语种 | 英语 |
WOS记录号 | WOS:000312466100009 |
内容类型 | 期刊论文 |
版本 | 出版稿 |
源URL | [http://202.127.25.143/handle/331003/555] |
专题 | 上海生化细胞研究所_上海生科院生化细胞研究所 |
推荐引用方式 GB/T 7714 | Runkle, EA,Zhang, HT,Cai, Z,et al. Reversion of the ErbB malignant phenotype and the DNA damage response[J]. EXPERIMENTAL AND MOLECULAR PATHOLOGY,2012,93(3):324-333. |
APA | Runkle, EA.,Zhang, HT.,Cai, Z.,Zhu, ZG.,Karger, BL.,...&Greene, MI.(2012).Reversion of the ErbB malignant phenotype and the DNA damage response.EXPERIMENTAL AND MOLECULAR PATHOLOGY,93(3),324-333. |
MLA | Runkle, EA,et al."Reversion of the ErbB malignant phenotype and the DNA damage response".EXPERIMENTAL AND MOLECULAR PATHOLOGY 93.3(2012):324-333. |
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