Abstract 2388: p73 - lncRNA Fer1l4 axis plays a critical role in suppression of cancer cell migration, invasion and metastasis in a p73-dependent manner via inhibition of miR-1273g-3p

A. Uboveja, Y. K. Satija, F. Siraj, Chanchal Bareja, D. Saluja
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Abstract

p73 is a member of the p53 tumor suppressor family and exerts its tumor suppressor functions by suppressing metastasis. It is increasingly evident that long noncoding RNAs (lncRNAs) play a significant role in tumor suppression. The present study is aimed to identify novel lncRNAs that play a role in p73-mediated suppression of metastasis in colorectal cancer cells. Transcriptome analysis was performed to detect the differentially expressed lncRNAs in presence and absence of p73. Out of these, FER1L4 lncRNA was found to be significantly induced in a p73-dependent manner. p73 binding to FER1L4 promoter was confirmed through bioinformatic analysis, luciferase reporter, ChIP and site-directed mutagenesis assays. Knockdown of FER1L4 and p73 significantly increased the invasion and migration rate of colorectal cancer cells as confirmed by wound-healing assay. Knockdown of FER1L4 decreased the expression of E-cadherin and increased the expression of prominent EMT markers such as N-cadherin, Snail, Vimentin and Fibronectin. FER1L4 causes a G2/M cell cycle arrest in a p73-dependent manner in HCT116p53-/-p73+/+ cells and upon FER1L4kd, normal cell cycle progression was observed. Annexin V/PI and TUNEL apoptosis assays revealed that FER1L4 induced apoptosis in HCT116p53-/-p73+/+ cells with increase in time-dependent treatment of etoposide and FER1L4kd inhibited apoptosis even in the presence of p73. The protein expression level of pro-apoptotic genes such as Bad, Bax, Bik, Bim, BID, Bak and PUMA decreased upon FER1L4kd and p73kd, confirming that FER1L4 plays a role in p73 mediated apoptosis and cell cycle arrest. FER1L4 also sponges the expression of miR-1273g-3p, thus inhibiting its oncogenic role. RNA-In situ hybridization (RNA-ISH) confirmed the decreased expression of p73 and FER1L4 mRNA in 30 human metastatic CRC tissues as compared to 30 human non-metastatic CRC tissues. Taken together, we provide conclusive proof that p73 exerts its anti-metastatic function by inducing the expression of lncRNA FER1L4 in response to genotoxic stress. Citation Format: Apoorva Uboveja, Yatendra Kumar Satija, Fouzia Siraj, Chanchal Bareja, Daman Saluja. p73 - lncRNA Fer1l4 axis plays a critical role in suppression of cancer cell migration, invasion and metastasis in a p73-dependent manner via inhibition of miR-1273g-3p [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 2388.
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摘要2388:p73- lncRNA Fer1l4轴通过抑制miR-1273g-3p,以p73依赖的方式在抑制癌细胞迁移、侵袭和转移中发挥关键作用
P73是p53肿瘤抑制家族的一员,通过抑制转移发挥其肿瘤抑制功能。长链非编码rna (long noncoding rna, lncRNAs)在肿瘤抑制中发挥着重要作用,这一点越来越明显。本研究旨在鉴定在p73介导的结直肠癌细胞转移抑制中发挥作用的新型lncRNAs。转录组分析检测p73存在和不存在时lncrna的差异表达。其中,FER1L4 lncRNA被发现以p73依赖的方式显著诱导。通过生物信息学分析、荧光素酶报告基因、ChIP和定点诱变实验证实p73与FER1L4启动子结合。经创面愈合实验证实,FER1L4和p73的下调可显著提高结直肠癌细胞的侵袭和迁移率。敲低FER1L4可降低E-cadherin的表达,增加N-cadherin、Snail、Vimentin和Fibronectin等EMT主要标志物的表达。在HCT116p53-/-p73+/+细胞中,FER1L4以p73依赖的方式引起G2/M细胞周期阻滞,在FER1L4kd后,观察到正常的细胞周期进展。Annexin V/PI和TUNEL细胞凋亡实验显示,随着依托opo苷处理时间的增加,FER1L4诱导HCT116p53-/-p73+/+细胞凋亡,即使p73存在,FER1L4kd也能抑制凋亡。在FER1L4kd和p73kd的作用下,Bad、Bax、Bik、Bim、BID、Bak、PUMA等促凋亡基因的蛋白表达水平下降,证实FER1L4在p73介导的细胞凋亡和细胞周期阻滞中起作用。FER1L4也抑制miR-1273g-3p的表达,从而抑制其致癌作用。rna原位杂交(RNA-ISH)证实30例转移性结直肠癌组织中p73和FER1L4 mRNA的表达低于30例非转移性结直肠癌组织。综上所述,我们提供了确凿的证据,证明p73通过诱导lncRNA FER1L4的表达来应对基因毒性应激,从而发挥其抗转移功能。引文格式:Apoorva Uboveja, Yatendra Kumar Satija, Fouzia Siraj, Chanchal Bareja, Daman Saluja。p73- lncRNA Fer1l4轴通过抑制miR-1273g-3p,以p73依赖的方式抑制癌细胞的迁移、侵袭和转移[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):摘要nr 2388。
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