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显示食管鳞状细胞癌中体细胞拷贝数改变以及mRNA和靶标微小RNA表达的复杂模式。

Shows Complex Patterns of Somatic Copy Number Alterations and Expressions of mRNAs and Target Micro RNAs in Esophageal Squamous Cell Carcinoma.

作者信息

Hu Nan, Wang Chaoyu, Zhang Tongwu, Su Hua, Liu Huaitian, Yang Howard H, Giffen Carol, Hu Ying, Taylor Philip R, Goldstein Alisa M

机构信息

Division of Cancer Epidemiology and Genetics (DCEG), National Cancer Institute (NCI), Bethesda, MD 20892, USA.

Center for Cancer Research (CCR), National Cancer Institute (NCI), Bethesda, MD 20892, USA.

出版信息

Cancers (Basel). 2022 Oct 13;14(20):5001. doi: 10.3390/cancers14205001.


DOI:10.3390/cancers14205001
PMID:36291785
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9599939/
Abstract

BACKGROUND: Human Cub and Sushi Multiple Domains 1 (CSMD1) is a novel candidate tumor-suppressor gene that codes for multiple domains, including complement regulatory and adhesion proteins, and has recently been shown to have alterations in multiple cancers. We investigated CSMD1 in esophageal squamous cell carcinoma (ESCC) by performing an integrated analysis on somatic copy number alterations (CNAs), including copy-number gain or loss, allelic imbalance (AI), loss of heterozygosity (LOH), and the expressions of mRNA and its target miRNAs on specimens from the same patients with ESCC. RESULTS: (i) Two-thirds of ESCC patients had all three types of alterations studied-somatic DNA alterations in 70%, and abnormal expressions of CSMD1 RNA in 69% and in target miRNAs in 66%; patterns among these alterations were complex. (ii) In total, 97% of 888 CSMD1 SNPs studied showed somatic DNA alterations, with most located near exons 4-11, 24-25, 39-40, 55-56, and 69-70. (iii) In total, 68% of SNPs with a CNA were correlated with expression of CSMD1. (iv) A total of 33 correlations between non-coding SNPs and expression of CSMD1 target miRs were found. CONCLUSIONS: Our results indicate that the gene may play a role in ESCC through complex patterns of DNA alterations and RNA and miRNA expressions. Alterations in some somatic SNPs in non-coding regions of appear to influence expression of this gene and its target miRNAs.

摘要

背景:人Cub和寿司多结构域蛋白1(CSMD1)是一种新型候选肿瘤抑制基因,编码包括补体调节蛋白和粘附蛋白在内的多个结构域,最近已证实在多种癌症中存在改变。我们通过对体细胞拷贝数改变(CNA)进行综合分析,包括拷贝数增加或减少、等位基因失衡(AI)、杂合性缺失(LOH)以及来自同一食管癌(ESCC)患者标本中mRNA及其靶标miRNA的表达,来研究CSMD1在食管鳞状细胞癌中的情况。 结果:(i)三分之二的ESCC患者存在所研究的所有三种类型的改变——70%的患者存在体细胞DNA改变,69%的患者CSMD1 RNA表达异常,66%的患者靶标miRNA表达异常;这些改变之间的模式很复杂。(ii)在总共研究的888个CSMD1单核苷酸多态性(SNP)中,97%显示体细胞DNA改变,大多数位于外显子4 - 11、24 - 25、39 - 40、55 - 56和69 - 70附近。(iii)总共68%的具有CNA的SNP与CSMD1的表达相关。(iv)总共发现了33个非编码SNP与CSMD1靶标miR表达之间的相关性。 结论:我们的结果表明,该基因可能通过复杂的DNA改变模式以及RNA和miRNA表达在ESCC中发挥作用。CSMD1非编码区某些体细胞SNP的改变似乎会影响该基因及其靶标miRNA的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca99/9599939/deca78781e90/cancers-14-05001-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca99/9599939/8df364ff8f0f/cancers-14-05001-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca99/9599939/39b911f19385/cancers-14-05001-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca99/9599939/c1c1b876f1b0/cancers-14-05001-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca99/9599939/46edcfc435fa/cancers-14-05001-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca99/9599939/a15856f7a49c/cancers-14-05001-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca99/9599939/deca78781e90/cancers-14-05001-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca99/9599939/8df364ff8f0f/cancers-14-05001-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca99/9599939/39b911f19385/cancers-14-05001-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca99/9599939/c1c1b876f1b0/cancers-14-05001-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca99/9599939/46edcfc435fa/cancers-14-05001-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca99/9599939/a15856f7a49c/cancers-14-05001-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca99/9599939/deca78781e90/cancers-14-05001-g006.jpg

相似文献

[1]
Shows Complex Patterns of Somatic Copy Number Alterations and Expressions of mRNAs and Target Micro RNAs in Esophageal Squamous Cell Carcinoma.

Cancers (Basel). 2022-10-13

[2]
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[3]
CSMD1 suppresses cancer progression by inhibiting proliferation, epithelial-mesenchymal transition, chemotherapy-resistance and inducing immunosuppression in esophageal squamous cell carcinoma.

Exp Cell Res. 2022-8-15

[4]
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[5]
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Cancer Biol Ther. 2009-5

[6]
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Cancer Cell Int. 2005-9-9

[7]
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[8]
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[9]
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[10]
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[2]
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本文引用的文献

[1]
Modified eQTL and Somatic DNA Segment Alterations in Esophageal Squamous Cell Carcinoma for Genes Related to Immunity, DNA Repair, and Inflammation.

Cancers (Basel). 2022-3-23

[2]
Mutational signatures in esophageal squamous cell carcinoma from eight countries with varying incidence.

Nat Genet. 2021-11

[3]
Integrated analysis of genome-wide miRNAs and targeted gene expression in esophageal squamous cell carcinoma (ESCC) and relation to prognosis.

BMC Cancer. 2020-5-6

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Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.

CA Cancer J Clin. 2018-9-12

[5]
An integrated view of the role of miR-130b/301b miRNA cluster in prostate cancer.

Exp Hematol Oncol. 2018-5-2

[6]
miR-10b exerts oncogenic activity in human hepatocellular carcinoma cells by targeting expression of CUB and sushi multiple domains 1 (CSMD1).

BMC Cancer. 2016-10-18

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Genomic Landscape of Somatic Alterations in Esophageal Squamous Cell Carcinoma and Gastric Cancer.

Cancer Res. 2016-4-1

[8]
Cancer statistics in China, 2015.

CA Cancer J Clin. 2016-1-25

[9]
Integrative genomics analysis of genes with biallelic loss and its relation to the expression of mRNA and micro-RNA in esophageal squamous cell carcinoma.

BMC Genomics. 2015-9-26

[10]
Toward understanding and exploiting tumor heterogeneity.

Nat Med. 2015-8

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