DNA repair and damage pathways in mesothelioma development and therapy

被引:11
|
作者
Malakoti, Faezeh [1 ]
Targhazeh, Niloufar [1 ]
Abadifard, Erfan [2 ,3 ]
Zarezadeh, Reza [1 ]
Samemaleki, Sahar [4 ]
Asemi, Zatollah [5 ]
Younesi, Simin [6 ]
Mohammadnejad, Reza [1 ]
Hossini, Seyed Hadi [1 ]
Karimian, Ansar [7 ]
Alemi, Forough [1 ]
Yousefi, Bahman [1 ]
机构
[1] Tabriz Univ Med Sci, Fac Med, Dept Biochem & Clin Labs, Tabriz, Iran
[2] Univ Tehran Med Sci, Sch Med, Tehran, Iran
[3] Univ Tehran Med Sci, Students Sci Res Ctr SSRC, Tehran, Iran
[4] Hamadan Univ Med Sci, Fac Med, Dept Immunol, Hamadan, Hamadan, Iran
[5] Kashan Univ Med Sci, Res Ctr Biochem & Nutr Metab Dis, Kashan, Iran
[6] RMIT Univ, Schoole Hlth & Biomed Sci, Melbourne, Vic, Australia
[7] Babol Univ Med Sci, Cellular & Mol Biol Res Ctr, Hlth Res Inst, Babol, Iran
关键词
Malignant mesothelioma; Malignant peritoneal mesothelioma; DNA damage repair; Signaling pathways; BRCA1 associated protein 1; BAP1; MALIGNANT PLEURAL MESOTHELIOMA; HOMOLOGOUS RECOMBINATION; SIGNALING PATHWAY; BAP1; CANCER; TRABECTEDIN; INHIBITION; GROWTH; SURVIVAL; CELLS;
D O I
10.1186/s12935-022-02597-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Malignant mesothelioma (MMe) is an aggressive neoplasm that occurs through the transformation of mesothelial cells. Asbestos exposure is the main risk factor for MMe carcinogenesis. Other important etiologies for MMe development include DNA damage, over-activation of survival signaling pathways, and failure of DNA damage response (DDR). In this review article, first, we will describe the most important signaling pathways that contribute to MMe development and their interaction with DDR. Then, the contribution of DDR failure in MMe progression will be discussed. Finally, we will review the latest MMe therapeutic strategies that target the DDR pathway.
引用
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页数:12
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