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参与DNA损伤反应/范可尼贫血信号传导的体细胞基因突变在人类实体瘤中具有组织和细胞类型特异性。

Somatic gene mutations involved in DNA damage response/Fanconi anemia signaling are tissue- and cell-type specific in human solid tumors.

作者信息

Rai Sudhir Kumar, Du Wei, Zhang Jun, Yu Herbert, Deng Youping, Fei Peiwen

机构信息

University of Hawaii Cancer Center, University of Hawaii, Honolulu, HI, United States.

John A. Burns School of Medicine, University of Hawaii, Honolulu, HI, United States.

出版信息

Front Med (Lausanne). 2024 Oct 3;11:1462810. doi: 10.3389/fmed.2024.1462810. eCollection 2024.

Abstract

With significant advancements in the study of DNA Damage Response (DDR) and Fanconi Anemia (FA) signaling, we previously introduced the term "FA signaling" to encompass "all signaling transductions involving one or more FA proteins." This network has now evolved into the largest cellular defense network, integrating over 30 key players, including ATM, ATR, BLM, HRR6, RAD18, FANCA, FANCB, FANCC, BRCA2, FANCD2, FANCE, FANCF, FANCG, FANCI, BRIP1, FANCL, FANCM, PALB2, RAD51C, SLX4, ERCC4, RAD51, BRCA1, UBE2T, XRCC2, MAD2L2, RFWD3, FAAP20, FAAP24, FAAP100, and CENPX. This system responds to both endogenous and exogenous cellular insults. However, the mutational signatures associated with this defense mechanism in non-FA human cancers have not been extensively explored. In this study, we report that different types of human cancers are characterized by distinct somatically mutated genes related to DDR/FA signaling, each accompanied by a unique spectrum of potential driver mutations. For example, in pan-cancer samples, ATM emerges as the most frequently mutated gene (5%) among the 31 genes analyzed, with the highest number of potential driver mutations (1714), followed by BRCA2 (4% with 970 putative driver mutations). However, this pattern is not universal across specific cancer types. For example, FANCT is the most frequently mutated gene in breast (14%) and liver (4%) cancers. In addition, the alteration frequency of DDR/FA signaling due to these mutations exceeds 70% in a subtype of prostate cancer, with each subtype of brain, breast, lung, and prostate cancers displaying distinct patterns of gene alteration frequency. Furthermore, these gene alteration patterns significantly impact patient survival and disease-free periods. Collectively, our findings not only enhance our understanding of cancer development and progression but also have significant implications for cancer patient care and prognosis, particularly in the development of effective therapeutic strategies.

摘要

随着DNA损伤反应(DDR)和范可尼贫血(FA)信号传导研究的重大进展,我们之前引入了“FA信号传导”一词,以涵盖“所有涉及一种或多种FA蛋白的信号转导”。这个网络现已发展成为最大的细胞防御网络,整合了30多个关键因子,包括ATM、ATR、BLM、HRR6、RAD18、FANCA、FANCB、FANCC、BRCA2、FANCD2、FANCE、FANCF、FANCG、FANCI、BRIP1、FANCL、FANCM、PALB2、RAD51C、SLX4、ERCC4、RAD51、BRCA1、UBE2T、XRCC2、MAD2L2、RFWD3、FAAP20、FAAP24、FAAP100和CENPX。该系统对内源性和外源性细胞损伤均有反应。然而,在非FA人类癌症中,与这种防御机制相关的突变特征尚未得到广泛研究。在本研究中,我们报告不同类型的人类癌症具有与DDR/FA信号传导相关的不同体细胞突变基因特征,每种癌症都伴有独特的潜在驱动突变谱。例如,在泛癌样本中,ATM是所分析的31个基因中最常发生突变的基因(5%),潜在驱动突变数量最多(1714个),其次是BRCA2(4%,有970个推定驱动突变)。然而,这种模式在特定癌症类型中并不普遍。例如,FANCT是乳腺癌(14%)和肝癌(4%)中最常发生突变的基因。此外,在一种前列腺癌亚型中,由于这些突变导致的DDR/FA信号传导改变频率超过70%,脑癌、乳腺癌、肺癌和前列腺癌的每个亚型都表现出不同的基因改变频率模式。此外,这些基因改变模式对患者生存和无病期有显著影响。总的来说,我们的发现不仅增进了我们对癌症发生发展的理解,而且对癌症患者的护理和预后具有重要意义,特别是在有效治疗策略的开发方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c56d/11483370/c403c5214975/fmed-11-1462810-g0001.jpg

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