Wang Meng-Yuan, Huang Man, Wang Chao-Yi, Tang Xiao-Ying, Wang Jian-Gen, Yang Yong-De, Xiong Xin, Gao Chao-Wei
Department of Breast Surgery, Chongqing University Three Gorges Hospital, Chongqing, China.
Front Oncol. 2021 Jun 15;11:682021. doi: 10.3389/fonc.2021.682021. eCollection 2021.
Triple-negative breast cancer (TNBC) is a highly aggressive cancer with poor prognosis. The lack of effective targeted therapies for TNBC remains a profound clinical challenge. Fusion transcripts play critical roles in carcinogenesis and serve as valuable diagnostic and therapeutic targets in cancer. The present study aimed to identify novel fusion transcripts in TNBC.
We analyzed the RNA sequencing data of 360 TNBC samples to identify and filter fusion candidates through SOAPfuse and ChimeraScan analysis. The characteristics, including recurrence, fusion type, chromosomal localization, TNBC subgroup distribution, and clinicopathological correlations, were analyzed in all candidates. Furthermore, we selected the promising fusion transcript and predicted its fusion type and protein coding capacity.
Using the RNA sequencing data, we identified 189 fusion transcripts in TNBC, among which 22 were recurrent fusions. Compared to para-tumor tissues, TNBC tumor tissues accumulated more fusion events, especially in high-grade tumors. Interestingly, these events were enriched at specific chromosomal loci, and the distribution pattern varied in different TNBC subtypes. The vast majority of fusion partners were discovered on chromosomes 1p, 11q, 19p, and 19q. Besides, fusion events mainly clustered on chromosome 11 in the immunomodulatory subtype and chromosome 19 in the luminal androgen receptor subtype of TNBC. Considering the tumor specificity and frameshift mutation, we selected as a novel biomarker and further validated it in TNBC samples using PCR and Sanger sequencing. Further, we successfully identified three types of (E6-E2, E5-E3, and E6-E3) and predicted the ORF of E6-E2, which could encode a protein of 712 amino acids, suggesting its critical role in TNBC.
Improved bioinformatic stratification and comprehensive analysis identified the fusion transcript as a novel biomarker with promising clinical application in the future.
三阴性乳腺癌(TNBC)是一种侵袭性很强且预后较差的癌症。TNBC缺乏有效的靶向治疗方法仍然是一个严峻的临床挑战。融合转录本在致癌过程中起关键作用,并且在癌症中作为有价值的诊断和治疗靶点。本研究旨在鉴定TNBC中的新型融合转录本。
我们分析了360例TNBC样本的RNA测序数据,通过SOAPfuse和ChimeraScan分析来鉴定和筛选融合候选物。对所有候选物的特征进行分析,包括复发情况、融合类型、染色体定位、TNBC亚组分布以及临床病理相关性。此外,我们选择了有前景的融合转录本并预测其融合类型和蛋白质编码能力。
利用RNA测序数据,我们在TNBC中鉴定出189个融合转录本,其中22个是复发性融合。与癌旁组织相比,TNBC肿瘤组织积累了更多的融合事件,尤其是在高级别肿瘤中。有趣的是,这些事件在特定的染色体位点富集,并且在不同的TNBC亚型中分布模式有所不同。绝大多数融合伙伴在染色体1p、11q、19p和19q上被发现。此外,融合事件主要聚集在TNBC免疫调节亚型的染色体11上以及腔面雄激素受体亚型的染色体19上。考虑到肿瘤特异性和移码突变,我们选择[具体内容缺失]作为一种新型生物标志物,并使用PCR和Sanger测序在TNBC样本中进一步验证它。此外,我们成功鉴定出三种类型的[具体内容缺失](E6-E2、E5-E3和E6-E3),并预测了E6-E2的开放阅读框,其可编码一个712个氨基酸的蛋白质,表明其在TNBC中的关键作用。
改进的生物信息分层和综合分析鉴定出融合转录本[具体内容缺失]作为一种新型生物标志物,在未来具有广阔的临床应用前景。