MicroRNAs(miRNAs), small non-coding RNAs, are involved in many aspects of biological processes. Previous studies have indicated that mi RNAs are important for hair follicle development and growth. In our study, we fou...MicroRNAs(miRNAs), small non-coding RNAs, are involved in many aspects of biological processes. Previous studies have indicated that mi RNAs are important for hair follicle development and growth. In our study, we found by q RT-PCR that miR-148 b was signi ficantly upregulated in sheep wool follicle bulbs in anagen phase compared with the telogen phase of the hair follicle cycle. Overexpression of miR-148 b promoted proliferation of both HHDPC and HHGMC. By using the TOPFlash system we demonstrated that miR-148 b could activate Wnt/β-catenin pathway and b-catenin, cyc D, c-jun and PPARD were consistently upregulated accordingly.Furthermore, transcript factor nuclear factor of activated T cells type 5(NFAT5) and Wnt10 b were predicted to be the target of mi R-148 b and this was substantiated using a Dual-Luciferase reporter system. Subsequently NFAT5 was further identi fied as the target of mi R-148 b using western blotting. These results were considered to indicate that mi R-148 b could activate the Wnt/β-catenin signal pathway by targeting NFAT5 to promote the proliferation of human hair follicle cells.展开更多
Objective This study aimed to examine the role of long non-coding RNA PCED1B antisense RNA 1(PCED1B-AS1)in the development of hepatocellular carcinoma(HCC).Methods A total of 62 pairs of HCC tissues and adjacent non-t...Objective This study aimed to examine the role of long non-coding RNA PCED1B antisense RNA 1(PCED1B-AS1)in the development of hepatocellular carcinoma(HCC).Methods A total of 62 pairs of HCC tissues and adjacent non-tumor tissues were obtained from 62 HCC patients.The interactions of PCED1B-AS1 and microRNA-34a(miR-34a)were detected by dual luciferase activity assay and RNA pull-down assay.The RNA expression levels of PCED1B-AS1,miR-34a and CD44 were detected by RT-qPCR,and the protein expression level of CD44 was determined by Western blotting.The cell proliferation was detected by cell proliferation assay,and the cell invasion and migration by transwell invasion assay.The HCC tumor growth after PCED1B-AS1 was downregulated was determined by in vivo animal study.Results PCED1B-AS1 was highly expressed in HCC tissues,which was associated with poor survival of HCC patients.Furthermore,PCED1B-AS1 interacted with miR-34a in HCC cells,but they did not regulate the expression of each other.Additionally,PCED1B-AS1 increased the expression level of CD44,which was targeted by miR-34a.The cell proliferation and invasion assay revealed that miR-34a inhibited the proliferation and invasion of HCC in vitro,while CD44 exhibited the opposite effects.Furthermore,PCED1B-AS1 suppressed the role of miR-34a.Moreover,the knockdown of PCED1B-AS1 repressed the HCC tumor growth in nude mice in vivo.Conclusion PCED1B-AS1 may play an oncogenic role by regulating the miR-34a/CD44 axis in HCC.展开更多
基金supported by grants from the National High Technology Research and Development Program of China(2013AA102506)Regional Project of National Natural Science Foundation of China (31360534)
文摘MicroRNAs(miRNAs), small non-coding RNAs, are involved in many aspects of biological processes. Previous studies have indicated that mi RNAs are important for hair follicle development and growth. In our study, we found by q RT-PCR that miR-148 b was signi ficantly upregulated in sheep wool follicle bulbs in anagen phase compared with the telogen phase of the hair follicle cycle. Overexpression of miR-148 b promoted proliferation of both HHDPC and HHGMC. By using the TOPFlash system we demonstrated that miR-148 b could activate Wnt/β-catenin pathway and b-catenin, cyc D, c-jun and PPARD were consistently upregulated accordingly.Furthermore, transcript factor nuclear factor of activated T cells type 5(NFAT5) and Wnt10 b were predicted to be the target of mi R-148 b and this was substantiated using a Dual-Luciferase reporter system. Subsequently NFAT5 was further identi fied as the target of mi R-148 b using western blotting. These results were considered to indicate that mi R-148 b could activate the Wnt/β-catenin signal pathway by targeting NFAT5 to promote the proliferation of human hair follicle cells.
基金supported by the Medical Science and Technology Research Foundation of Guangdong Province(No.A2020559).
文摘Objective This study aimed to examine the role of long non-coding RNA PCED1B antisense RNA 1(PCED1B-AS1)in the development of hepatocellular carcinoma(HCC).Methods A total of 62 pairs of HCC tissues and adjacent non-tumor tissues were obtained from 62 HCC patients.The interactions of PCED1B-AS1 and microRNA-34a(miR-34a)were detected by dual luciferase activity assay and RNA pull-down assay.The RNA expression levels of PCED1B-AS1,miR-34a and CD44 were detected by RT-qPCR,and the protein expression level of CD44 was determined by Western blotting.The cell proliferation was detected by cell proliferation assay,and the cell invasion and migration by transwell invasion assay.The HCC tumor growth after PCED1B-AS1 was downregulated was determined by in vivo animal study.Results PCED1B-AS1 was highly expressed in HCC tissues,which was associated with poor survival of HCC patients.Furthermore,PCED1B-AS1 interacted with miR-34a in HCC cells,but they did not regulate the expression of each other.Additionally,PCED1B-AS1 increased the expression level of CD44,which was targeted by miR-34a.The cell proliferation and invasion assay revealed that miR-34a inhibited the proliferation and invasion of HCC in vitro,while CD44 exhibited the opposite effects.Furthermore,PCED1B-AS1 suppressed the role of miR-34a.Moreover,the knockdown of PCED1B-AS1 repressed the HCC tumor growth in nude mice in vivo.Conclusion PCED1B-AS1 may play an oncogenic role by regulating the miR-34a/CD44 axis in HCC.
