Comprehensive RNA-seq analysis of alternative splicing events that distinguishes between metastatic oral cancer of gingiva and tongue
محل انتشار: مجله سرطان شناسی و علوم پزشکی، دوره: 2، شماره: 1
سال انتشار: 1401
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 280
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استخراج به نرم افزارهای پژوهشی:
شناسه ملی سند علمی:
JR_JCOMS-2-1_007
تاریخ نمایه سازی: 28 تیر 1402
چکیده مقاله:
Introduction:
Oral cancer (OC) is a multifactorial disease caused due to various genomic changes. Alternative splicing
(AS) is a regulatory genetic process through which messenger RNA forms diverse protein variants. This study a ims to
study the variation in the AS events at tongue and gingiva locations of OC.
Materials and Methods: FortyForty-five paired end OC RNA RNA-seq data were downloaded from Sequence Read Archive (SRA)
data repository. Twenty four paired end OC (tongue ۱۳, gingival ۱۱) RNA sequences passed the stringent inclusion/
exclusion criteria which were analyzed foll owing Tuxedo pipeline. The ClueGO (v۲.۵.۸) tool in Cytoscape app manager
(v۳.۷.۱) was used for gene set enrichment analysis keeping false discovery rate (FDR <=۰.۰۵).
Results:
EightyEighty-three genes were identified to be signific antly alternatively spliced when comparison was made between
RNA sequences from normal tissues and tumor tissues from the gingiva region (p<۰.۰۵). Similarly, ۳۹ genes were found
to be significantly alternatively spliced when comparison was made between nor mal tissues and tumor tissues from tongue
region of OC. Of these, only ۴ genes i.e. AHRAHR, AL۳۵۶۴۸۸AL۳۵۶۴۸۸.۲ , KREMEN۱KREMEN۱, SH۳TC۱ were similar in gingiva and tongue
whereas others were unique to their location location.
Conclusion:
GenomeGenome-wide AS events vary considerably in gingival and to ngue locations of OC. Hence, these events
need to be thoroughly investigated for defining the treatment strategy. Further functional studies are needed to decipher
the role of AS in OC OC.
کلیدواژه ها:
نویسندگان
Vishwas Sharma
Division of Cytopathology, ICMR-National Institute of Cancer Prevention and Research, Noida, Uttar Pradesh, India
Dinesh Kumar
ICMR-National Institute of Cancer Prevention and Research, Noida, Uttar Pradesh, India
Harpreet Singh
Informatics, Sy stems & Research Management (ISRM), ICMR, New Delhi
Sanjay Gupta
Division of Cytopathology, ICMR-National Institute of Cancer Prevention and Research, Noida, Uttar Pradesh, India