Protrusion-localized STAT3 mRNA promotes metastasis of highly metastatic hepatocellular carcinoma cells in vitro

• Published in: Acta pharmacologica Sinica Vol. 37; no. 6; pp. 805 - 813
• Main Authors: Liu, Yan-hong, Jin, Jia-lu, Wang, Yu-zhe, Tan, Ying, Zhou, Ying-ying, Peng, Ting, Li, Feng, Liang, Wan-dong, Chartrand, Pascal, Jiang, Yu-yang, Shen, Zhi-fa
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.06.2016; Nature Publishing Group
• Subjects: Biomedical and Life Sciences; Biomedicine; Carcinoma, Hepatocellular - genetics; Carcinoma, Hepatocellular - pathology; Cell Line, Tumor; Cell Movement; Humans; Immunology; Internal Medicine; Liver - metabolism; Liver - pathology; Liver Neoplasms - genetics; Liver Neoplasms - pathology; Medical Microbiology; mRNA定位; Neoplasm Invasiveness - genetics; Neoplasm Invasiveness - pathology; Neoplasm Metastasis - genetics; Neoplasm Metastasis - pathology; Original; original-article; Pharmacology/Toxicology; RNA, Messenger - analysis; RNA, Messenger - genetics; SMMC-7721细胞; STAT3; STAT3 Transcription Factor - genetics; Vaccine; 体外; 本地化; 突出; 肝癌细胞; 血小板衍生生长因子; mRNA localization; metastasis; SMMC-7721 cells; STAT3; platelet-derived growth factor receptor; Boyden chamber assay; HCCLM3 cells; hepatocellular carcinoma
• ISSN: 1671-4083; 1745-7254
• DOI: 10.1038/aps.2015.166

Aim： Recent evidence shows that localization of mRNAs and their protein products at cellular protrusions plays a decisive function in the metastasis of cancer cells. The aim of this study was to identify the variety of proteins encoded by protrusion-localized mRNAs and their roles in the metastasis and invasion of liver cancer cells. Methods： Highly metastatic hepatocellular carcinoma cell line HCCLM3 and non-metastatic hepatocellular carcinoma cell line SMMC-7721 were examined. Cell protrusions （Ps） were separated from cell bodies （CB） using a Boyden chamber assay; total mRNA population in CB and Ps fractions was analyzed using high-throughput direct RNA sequencing. The localization of STAT3 mRNA and protein at Ps was confirmed using RT-qPCR, RNA FISH, and immunofluorescence assays. Cell migration capacity and invasiveness of HCCLM3 cells were evaluated using MTT, wound healing migration and in vitro invasion assays. The interaction between Stat3 and growth factor receptors was explored with co-immunoprecipitation assays. Results： In HCCLM3 cells, 793 mRNAs were identified as being localized in the Ps fraction according to a cut-off value （Ps/CB ratio） 〉1.6. The Ps-localized mRNAs could be divided into 4 functional groups, and were all closely related to the invasive and metastatic properties. STAT3 mRNA accumulated in the Ps of HCCLM3 cells compared with non-metastatic SMMC-7721 cells. Treatment of HCCLM3 cells with siRNAs against STAT3 mRNA drastically decreased the cell migration and invasion. Moreover, Ps-localized Stat3 was found to interact with pseudopod-enriched platelet-derived growth factor receptor tyrosine kinase （PDGFRTK） in a growth factor- dependent manner. Conclusion： This study reveals STAT3 mRNA localization at the Ps of metastatic hepatocellular carcinoma HCCLM3 cells by combining application of genome-wide and gene specific description and functional analysis.