Overexpression of TSPAN8 in consensus molecular subtype 3 colorectal cancer

IF 2.8 4区 医学 Q2 PATHOLOGY Experimental and molecular pathology Pub Date : 2024-06-01 DOI:10.1016/j.yexmp.2024.104911
Thanawat Suwatthanarak , Pariyada Tanjak , Amphun Chaiboonchoe , Onchira Acharayothin , Kullanist Thanormjit , Jantappapa Chanthercrob , Tharathorn Suwatthanarak , Apichaya Niyomchan , Masayoshi Tanaka , Mina Okochi , Ananya Pongpaibul , Wipapat Vicki Chalermwai , Atthaphorn Trakarnsanga , Asada Methasate , Manop Pithukpakorn , Vitoon Chinswangwatanakul
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Abstract

Background

Recently, consensus molecular subtypes (CMSs) have been proposed as a robust transcriptome-based classification system for colorectal cancer (CRC). Tetraspanins (TSPANs) are transmembrane proteins. They have been associated with the development of numerous malignancies, including CRC, through their role as “master organizers” for multi-molecular membrane complexes. No previous study has investigated the correlation between TSPANs and CMS classification. Herein, we investigated the expression of TSPANs in patient-derived primary CRC tissues and their CMS classifications.

Methods

RNA samples were derived from primary CRC tissues (n = 100 patients diagnosed with colorectal adenocarcinoma) and subjected to RNA sequencing for transcriptome-based CMS classification and TSPAN-relevant analyses. Immunohistochemistry (IHC) and immunofluorescence (IF) stains were conducted to observe the protein expression level. To evaluate the relative biological pathways, gene-set enrichment analysis was performed.

Results

Of the highly expressed TSPAN genes in CRC tissues (TSPAN8, TSPAN29, and TSPAN30), TSPAN8 was notably overexpressed in CMS3-classified primary tissues. The overexpression of TSPAN8 protein in CMS3 CRC was also observed by IHC and IF staining. As a result of gene-set enrichment analysis, TSPAN8 may potentially play a role in organizing signaling complexes for kinase-based metabolic deregulation in CMS3 CRC.

Conclusions

The present study reports the overexpression of TSPAN8 in CMS3 CRC. This study proposes TSPAN8 as a subtype-specific biomarker for CMS3 CRC. This finding provides a foundation for future CMS-based studies of CRC, a complex disease and the second leading cause of cancer mortality worldwide.

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共识分子亚型 3 结直肠癌中 TSPAN8 的过度表达
背景最近,有人提出了共识分子亚型(CMS),作为基于转录组的结直肠癌(CRC)稳健分类系统。四跨蛋白(TSPANs)是一种跨膜蛋白。它们作为多分子膜复合物的 "主组织者",与包括 CRC 在内的多种恶性肿瘤的发病有关。以前没有研究调查过 TSPANs 与 CMS 分类之间的相关性。方法从原发性 CRC 组织(n = 100 名确诊为结直肠腺癌的患者)中提取 RNA 样本,并对其进行 RNA 测序,以进行基于转录组的 CMS 分类和 TSPAN 相关分析。免疫组化(IHC)和免疫荧光(IF)染色用于观察蛋白质表达水平。结果 在 CRC 组织中高表达的 TSPAN 基因(TSPAN8、TSPAN29 和 TSPAN30)中,TSPAN8 在 CMS3 分类的原发性组织中明显过表达。IHC 和 IF 染色也观察到 TSPAN8 蛋白在 CMS3 CRC 中的过表达。通过基因组富集分析,TSPAN8 有可能在 CMS3 CRC 中起到组织信号复合物的作用,从而导致基于激酶的代谢失调。本研究提出 TSPAN8 是 CMS3 CRC 的亚型特异性生物标志物。这一发现为未来基于 CMS 的 CRC 研究奠定了基础,CRC 是一种复杂的疾病,也是全球癌症死亡的第二大原因。
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来源期刊
CiteScore
8.90
自引率
0.00%
发文量
78
审稿时长
11.5 weeks
期刊介绍: Under new editorial leadership, Experimental and Molecular Pathology presents original articles on disease processes in relation to structural and biochemical alterations in mammalian tissues and fluids and on the application of newer techniques of molecular biology to problems of pathology in humans and other animals. The journal also publishes selected interpretive synthesis reviews by bench level investigators working at the "cutting edge" of contemporary research in pathology. In addition, special thematic issues present original research reports that unravel some of Nature''s most jealously guarded secrets on the pathologic basis of disease. Research Areas include: Stem cells; Neoangiogenesis; Molecular diagnostics; Polymerase chain reaction; In situ hybridization; DNA sequencing; Cell receptors; Carcinogenesis; Pathobiology of neoplasia; Complex infectious diseases; Transplantation; Cytokines; Flow cytomeric analysis; Inflammation; Cellular injury; Immunology and hypersensitivity; Athersclerosis.
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