Suppr超能文献

急性髓系白血病的预后:核苷酸切除修复多态性在中危患者中的作用。

Acute myeloid leukemia outcome: role of nucleotide excision repair polymorphisms in intermediate risk patients.

机构信息

Epidemiology, University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Leuk Lymphoma. 2010 Apr;51(4):598-605. doi: 10.3109/10428190903582804.

Abstract

In acute myeloid leukemia (AML), cytogenetics predicts treatment outcome for the favorable and poor subgroups but not for the intermediate subgroup. Polymorphisms within the nucleotide excision repair (NER) pathway may lead to interindividual differences in DNA repair capacity, influencing outcome. We studied the role of six polymorphisms (ERCC1 Gln504Lys, XPD Lys751Gln, XPC Ala499Val, XPC Lys939Gln, XPG Asp1104His, and CCNH Val270Ala) in overall and disease-free survival among 170 adult de novo patients with intermediate cytogenetics (diploid [n = 117]; non-diploid [n = 53]), treated with induction chemotherapy. Kaplan-Meier and Cox proportional hazards models were performed. Diploid patients with the XPD AC/CC genotype survived shorter than those with the wild-type genotype (median survival 22 vs. 40 months, p = 0.03). Diploid patients with XPC CT/TT genotype survived shorter than those with the wild-type genotype (median survival 15 vs. 30 months, p = 0.02). After adjusting for clinical and sociodemographic variables, patients carrying both XPD AC/CC and XPC CT/TT had a greater than two-fold increased risk of dying, compared to those with the wild-type genotypes (HR = 2.49; 95% CI: 1.06-5.85). No associations were observed for disease-free survival. This combined genotype may modulate treatment effect, decreasing overall survival. These findings could in the future help select treatments for patients with normal cytogenetics.

摘要

在急性髓系白血病(AML)中,细胞遗传学可预测有利和不良亚组的治疗结果,但不能预测中间亚组的结果。核苷酸切除修复(NER)途径中的多态性可能导致个体间 DNA 修复能力的差异,从而影响结果。我们研究了六个多态性(ERCC1 Gln504Lys、XPD Lys751Gln、XPC Ala499Val、XPC Lys939Gln、XPG Asp1104His 和 CCNH Val270Ala)在 170 名中间细胞遗传学(二倍体 [n = 117];非二倍体 [n = 53])的成年初治 AML 患者的总生存和无病生存中的作用,这些患者接受诱导化疗。进行了 Kaplan-Meier 和 Cox 比例风险模型分析。XPD AC/CC 基因型的二倍体患者的生存时间短于野生型基因型(中位生存时间 22 与 40 个月,p = 0.03)。XPC CT/TT 基因型的二倍体患者的生存时间短于野生型基因型(中位生存时间 15 与 30 个月,p = 0.02)。在校正了临床和社会人口统计学变量后,与野生型基因型相比,携带 XPD AC/CC 和 XPC CT/TT 的患者死亡风险增加了两倍以上(HR = 2.49;95%CI:1.06-5.85)。无病生存无相关性。这种联合基因型可能调节治疗效果,降低总生存。这些发现将来可能有助于为正常细胞遗传学的患者选择治疗方法。

相似文献

3
Polymorphisms in XPC, XPD and XPG DNA repair genes and leukemia risk in a Tunisian population.
Leuk Lymphoma. 2015 Jun;56(6):1856-62. doi: 10.3109/10428194.2014.974045. Epub 2014 Nov 14.
7
Genetic variants of nucleotide excision repair pathway and outcomes of induction therapy in acute myeloid leukemia.
Per Med. 2019 Nov;16(6):479-490. doi: 10.2217/pme-2018-0077. Epub 2019 Oct 24.
9
Polymorphisms in nucleotide excision repair genes and susceptibility to colorectal cancer in the Polish population.
Mol Biol Rep. 2015 Mar;42(3):755-64. doi: 10.1007/s11033-014-3824-z. Epub 2014 Nov 13.
10
Polymorphisms of nucleotide excision repair genes predict melanoma survival.
J Invest Dermatol. 2013 Jul;133(7):1813-21. doi: 10.1038/jid.2012.498. Epub 2013 Feb 14.

引用本文的文献

2
The Role of DNA Repair (, , , and Gene Polymorphisms in the Development of Myeloproliferative Neoplasms.
Medicina (Kaunas). 2024 Mar 19;60(3):506. doi: 10.3390/medicina60030506.
3
Structural modeling and analyses of genetic variations in the human XPC nucleotide excision repair protein.
J Biomol Struct Dyn. 2023;41(23):13535-13562. doi: 10.1080/07391102.2023.2177349. Epub 2023 Mar 8.
4
Xeroderma Pigmentosum Complementation Group C (XPC): Emerging Roles in Non-Dermatologic Malignancies.
Front Oncol. 2022 Apr 21;12:846965. doi: 10.3389/fonc.2022.846965. eCollection 2022.
6
DNMT3A Harboring Leukemia-Associated Mutations Directs Sensitivity to DNA Damage at Replication Forks.
Clin Cancer Res. 2022 Feb 15;28(4):756-769. doi: 10.1158/1078-0432.CCR-21-2863.
7
Xeroderma pigmentosum and acute myeloid leukemia: a case report.
J Med Case Rep. 2021 Aug 26;15(1):437. doi: 10.1186/s13256-021-02969-1.
8
Genetic variants of nucleotide excision repair pathway and outcomes of induction therapy in acute myeloid leukemia.
Per Med. 2019 Nov;16(6):479-490. doi: 10.2217/pme-2018-0077. Epub 2019 Oct 24.
9
HSP90 inhibition depletes DNA repair proteins to sensitize acute myelogenous leukemia to nucleoside analog chemotherapeutics.
Leuk Lymphoma. 2019 Sep;60(9):2308-2311. doi: 10.1080/10428194.2019.1571197. Epub 2019 Feb 18.

本文引用的文献

1
Associations between XPC polymorphisms and risk of cancers: A meta-analysis.
Eur J Cancer. 2008 Oct;44(15):2241-53. doi: 10.1016/j.ejca.2008.06.024. Epub 2008 Sep 2.
4
The Interaction of Selection and Linkage. I. General Considerations; Heterotic Models.
Genetics. 1964 Jan;49(1):49-67. doi: 10.1093/genetics/49.1.49.
5
Polymorphisms in DNA repair genes and therapeutic outcomes of AML patients from SWOG clinical trials.
Blood. 2007 May 1;109(9):3936-44. doi: 10.1182/blood-2006-05-022111. Epub 2006 Dec 29.
6
Genomic polymorphisms provide prognostic information in intermediate-risk acute myeloblastic leukemia.
Blood. 2006 Jun 15;107(12):4871-9. doi: 10.1182/blood-2005-08-3272. Epub 2006 Feb 28.
8
Drug therapy for acute myeloid leukemia.
Blood. 2005 Aug 15;106(4):1154-63. doi: 10.1182/blood-2005-01-0178. Epub 2005 May 3.
9
Genetic variation in XPD predicts treatment outcome and risk of acute myeloid leukemia following chemotherapy.
Blood. 2004 Dec 15;104(13):3872-7. doi: 10.1182/blood-2004-06-2161. Epub 2004 Aug 31.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验