The association between early-onset cardiac events caused by neoadjuvant or adjuvant chemotherapy in triple-negative breast cancer patients and some novel autophagy-related polymorphisms in their genomic DNA: a real-world study

被引:19
|
作者
Liu, Binliang [1 ,2 ]
An, Tao [2 ,3 ]
Li, Meiying [4 ]
Yi, Zongbi [1 ,2 ]
Li, Chunxiao [2 ,5 ]
Sun, Xiaoying [6 ]
Guan, Xiuwen [1 ,2 ]
Li, Lixi [1 ,2 ]
Wang, Yanfeng [2 ,7 ]
Zhang, Yuhui [3 ]
Xu, Binghe [1 ,2 ]
Ma, Fei [1 ,2 ]
Zeng, Yixin [2 ,8 ,9 ]
机构
[1] Chinese Acad Med Sci, Canc Hosp, Natl Clin Res Ctr Canc, Dept Med Oncol,Natl Canc Ctr, Beijing 100021, Peoples R China
[2] Peking Union Med Coll, Beijing 100021, Peoples R China
[3] Chinese Acad Med Sci, Natl Ctr Cardiovasc Dis, Fuwai Hosp, State Key Lab Cardiovasc Dis,Heart Failure Ctr, Beijing 100037, Peoples R China
[4] Shandong Univ, Shandong Canc Hosp & Inst, Jinan 250117, Shandong, Peoples R China
[5] Chinese Acad Med Sci, Canc Inst Hosp, State Key Lab Mol Oncol, Beijing 100021, Peoples R China
[6] Canc Hosp Huanxing, Dept Med Oncol, Beijing 100065, Peoples R China
[7] Chinese Acad Med Sci, Canc Hosp, Natl Canc Ctr, Dept Comprehens Oncol, Beijing 100021, Peoples R China
[8] Chinese Acad Med Sci, Beijing 100730, Peoples R China
[9] Sun Yat Sen Univ, Canc Ctr, State Key Lab Oncol South China, Collaborat Innovat Ctr Canc Med, 651 Dongfeng Rd East, Guangzhou 510060, Guangdong, Peoples R China
来源
CANCER COMMUNICATIONS | 2018年 / 38卷
基金
中国国家自然科学基金;
关键词
Triple-negative breast cancer; Chemotherapy; Cardiotoxicity; Autophagy; Single nucleotide polymorphisms; RESTING HEART-RATE; ANTHRACYCLINE-INDUCED CARDIOTOXICITY; ALL-CAUSE MORTALITY; PREVENTION; SURVIVORS; TOXICITY;
D O I
10.1186/s40880-018-0343-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background An increasing number of cancer patients die of cardiovascular diseases. The cardiotoxicity of chemotherapy is particularly important in triple-negative breast cancer (TNBC) with limited therapeutic options. Cardiac autophagy is an important mechanism of cardiotoxicity. This research was aimed to investigate the cardiotoxicity of chemotherapy in TNBC, screen the susceptible population, and determine the relationship between cardiotoxicity and autophagy-related polymorphisms. Methods: From a total of 2450 stage I-III TNBC patients, 147 met the inclusion criteria and finally recruited. Electrocardiography (ECG) was performed before most chemotherapy cycles, and echocardiography (UCG) was performed according to clinical needs. All ECG and UCG records were re-interpreted by cardiologists at the National Center for Cardiovascular Disease, Fuwai Hospital. According to the National Center for Biotechnology Information and the Catalog of Somatic Mutations in Cancer database, we selected 25 single nucleotide polymorphisms (SNPs) related to autophagy and genotyped the 147 TNBC patients. Paired-sample T tests, Chi squared tests, and logistic regression models were employed for the analysis. Results: Only 46 (31.3%) patients had normal ECG records after every chemotherapy cycle. Among the 16 patients who underwent UCG, 2 (12.5%) had a reversible decrease of left ventricular ejection fraction. The use of anthracyclines and excessive alcohol consumption were risk factors of ECG abnormalities. With the continuation of chemotherapy, heart rate gradually increased. Anthracyclines were associated with QRS duration abnormalities (P=0.043). After genotyping for 25 autophagy-related SNPs, we found that the G allele of autophagy-related 13 (ATG13) rs10838611 was significantly associated with ECG abnormalities (odds ratio=2.258, 95% confidence interval=1.318-3.869; P=0.003). Conclusion: ECG abnormalities caused by chemotherapy are common in the real world. Autophagy-related SNPs are associated with chemotherapy-induced cardiotoxicity, thereby providing new evidence for autophagy as a cause of chemotherapy-induced cardiac damage.
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页数:11
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