NFκB (ReIA) mediates transactivation of hnRNPD in oral cancer cells

被引:9
作者
Kumar, Vikas [1 ]
Kumar, Anurag [1 ]
Kumar, Manish [2 ]
Lone, Moien Rasheed [1 ]
Mishra, Deepika [3 ]
Chauhan, Shyam Singh [1 ]
机构
[1] All India Inst Med Sci, Dept Biochem, New Delhi, India
[2] All India Inst Med Sci, Dept Biochem, Bilaspur, India
[3] All India Inst Med Sci, Ctr Dent Educ & Res, Div Oral Pathol, New Delhi, India
关键词
ARE/POLY(U)-BINDING FACTOR-1 AUF1; GENE-EXPRESSION; PROTEIN; TRANSCRIPTION; ACTIVATION; PROMOTER; IDENTIFICATION; INHIBITION; CYTOKINES; LINKING;
D O I
10.1038/s41598-022-09963-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Heterogeneous Ribonucleoprotein D (hnRNPD) is an RNA binding protein involved in post-transcriptional regulation of multiple mediators of carcinogenesis. We previously demonstrated a strong association of hnRNPD over expression with poor outcome in Oral Squamous Cell Carcinoma (OSCC). However, hitherto the precise molecular mechanism of its overexpression in oral cancer was not clear. Therefore, in an attempt to elucidate the transcriptional regulation of hnRNPD expression, we cloned 1406 bp of 5' flanking region of human hnRNPD gene along with 257 bp of its first exon upstream to promoterless luciferase reporter gene in pGL3-Basic. Transfection of the resulting construct in SCC-4 cells yielded 1271 fold higher luciferase activity over parent vector. By promoter deletion analysis, we identified a canonical TATA box containing 126 bp core promoter region that retained - 58% activity of the full length promoter. In silico analysis revealed the presence of four putative NF kappa B binding motifs in the promoter. Sequential deletion of these motifs from the full-length promoter reporter construct coupled with luciferase assays revealed an 82% decrease in promoter activity after deletion of the first (-1358/-1347) motif and 99% reduction after the deletion of second motif (-1052/-1041). In-vivo binding of NF kappa B (ReIA) to these two motifs in SCC-4 cells was confirmed by ChIP assays. Site directed mutagenesis of even one of these two motifs completely abolished promoter activity, while mutagenesis of the remaining two motifs had marginal effect on the same. Consistent with these findings, treatment of SCC-4 cells with PDTC, a known inhibitor of NF kappa B dramatically reduced the levels hnRNPD mRNA and protein. Finally, the expression of hnRNPD and NF kappa B in clinical specimen from 37 oral cancer patients was assessed and subjected to Spearmen's Correlation analysis which revealed a strong positive correlation between the two. Thus, results of the present study for the first time convincingly demonstrate NF kappa B (ReIA) mediated transcriptional upregulation of hnRNPD expression in oral cancer.
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页数:15
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