Super-enhancer-driven ameboidal-type cell migration-related MMP14 expression in tongue squamous cell carcinoma switched by BATF and ATF3

Author:

Shi Zhimin1,Wang Rui2,Huang Jie2,Qian Qian3,Hu Menglin24,Zhang Hengguo2ORCID,Feng Linfei5,Gu Hao1,Wang Yuanyin2ORCID

Affiliation:

1. Department of Immunology, the School of Basic Medical Sciences, Anhui Medical University , Hefei 230032 , China

2. Key Laboratory of Oral Diseases Research of Anhui Province, College & Hospital of Stomatology, Anhui Medical University , Hefei 230032 , China

3. Department of Pharmacy, The First Affiliated Hospital of Anhui University of Chinese Medicine , Hefei 230022 , China

4. Department of Dental, Tongling Traditional Chinese Medicine Hospital , Taipinghu Road, Tongling 244000 , China

5. Department of Oral and Maxillofacial Surgery, The First Affiliated Hospital of Anhui Medical University , Hefei 230032 , China

Abstract

Abstract Background Tongue squamous cell carcinoma (TSCC) exhibits an aggressive biological behavior of lymph node and distant metastasis, which contributes to poorer prognosis and results in tongue function loss or death. In addition to known regulators and pathways of cell migration in TSCC, it is important to uncover pivotal switches governing tumor metastasis. Methods Cancer cell migration-associated transcriptional and epigenetic characteristics were profiled in TSCC, and the specific super-enhancers (SEs) were identified. Molecular function and mechanism studies were used to investigate the pivotal switches in TSCC metastasis. Results Ameboidal-type cell migration-related genes accompanied by transcriptional and epigenetic activity were enriched in TSCC. Meanwhile, the higher-ranked SE-related genes showed significant differences between 43 paired tumor and normal samples from the TCGA TSCC cohort. In addition, key motifs were detected in SE regions, and transcription factor-related expression levels were significantly associated with TSCC survival status. Notably, BATF and ATF3 regulated the expression of ameboidal-type cell migration-related MMP14 by switching the interaction with the SE region. Conclusion SEs and related key motifs transcriptional regulate tumor metastasis-associated MMP14 and might be potential therapeutic targets for TSCC.

Funder

Basic and Clinical Cooperative Research

Anhui Medical University

natural science research projects in universities in Anhui Province

Publisher

Oxford University Press (OUP)

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