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thle 2 crl 2706 normal human liver epithelial cell line  (ATCC)


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    ATCC thle 2 crl 2706 normal human liver epithelial cell line
    Thle 2 Crl 2706 Normal Human Liver Epithelial Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 648 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+normal+liver+epithelial+cell+line+thle+2/THLE-2/pm41977432-139-19-30
    Average 98 stars, based on 648 article reviews
    thle 2 crl 2706 normal human liver epithelial cell line - by Bioz Stars, 2026-10
    98/100 stars

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    Planar Chromatography:

    Article Title: Knockdown of terminal differentiation induced ncRNA (TINCR) suppresses proliferation and invasion in hepatocellular carcinoma by targeting the miR-218-5p/DEAD-box helicase 5 (DDX5) axis.
    Article Snippet: Funding information Henan Medical Science and Technology Research Program, Grant/Award Number: SBGJ2018071 Abstract Terminal differentiation induced ncRNA (TINCR), a newly identified lncRNA, has been found to be associated with different human cancers including hepatocellular carcinoma (HCC).. However, little is known regarding the pathological mechanisms of TINCR in HCC progression.. In this study, we confirmed that TINCR expression was upregulated in HCC tumors and cell lines, and high TINCR expression was associated with larger tumor size, advanced tumor node metastasis stage, and poor prognosis.



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    RNPEP was overexpressed in hepatocellular carcinoma (HCC) tumors and cell lines. (A) RNPEP expression levels in human cancers in accordance with the data from Timer 2.0. (B) RNPEP expression levels in normal, HCC tumor and HCC metastatic tissues according to the data from the TNM plot. (C) RNPEP mRNA levels in normal human liver <t>epithelial</t> cells (THLE‐2), low‐metastatic HCC cells (MHCC‐97L), and high‐metastatic HCC cells (HCC‐LM3 and MHCC‐97H). Data were acquired by the real‐time PCR analysis and presented as mean ± SD, n = 3/group, * p < 0.05, ** p < 0.01. (D) RNPEP concentrations in cell supernatant of THLE‐2, MHCC‐97L, HCC‐LM3 and MHCC‐97H. Data were acquired by ELISA, and presented as the mean ± SD, n = 3/group, * p < 0.05, ** p < 0.01, *** p < 0.001.
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    RNPEP was overexpressed in hepatocellular carcinoma (HCC) tumors and cell lines. (A) RNPEP expression levels in human cancers in accordance with the data from Timer 2.0. (B) RNPEP expression levels in normal, HCC tumor and HCC metastatic tissues according to the data from the TNM plot. (C) RNPEP mRNA levels in normal human liver epithelial cells (THLE‐2), low‐metastatic HCC cells (MHCC‐97L), and high‐metastatic HCC cells (HCC‐LM3 and MHCC‐97H). Data were acquired by the real‐time PCR analysis and presented as mean ± SD, n = 3/group, * p < 0.05, ** p < 0.01. (D) RNPEP concentrations in cell supernatant of THLE‐2, MHCC‐97L, HCC‐LM3 and MHCC‐97H. Data were acquired by ELISA, and presented as the mean ± SD, n = 3/group, * p < 0.05, ** p < 0.01, *** p < 0.001.

    Journal: Cancer Science

    Article Title: Tumor exosomal RNPEP promotes lung metastasis of liver cancer via inducing cancer‐associated fibroblast activation

    doi: 10.1111/cas.16417

    Figure Lengend Snippet: RNPEP was overexpressed in hepatocellular carcinoma (HCC) tumors and cell lines. (A) RNPEP expression levels in human cancers in accordance with the data from Timer 2.0. (B) RNPEP expression levels in normal, HCC tumor and HCC metastatic tissues according to the data from the TNM plot. (C) RNPEP mRNA levels in normal human liver epithelial cells (THLE‐2), low‐metastatic HCC cells (MHCC‐97L), and high‐metastatic HCC cells (HCC‐LM3 and MHCC‐97H). Data were acquired by the real‐time PCR analysis and presented as mean ± SD, n = 3/group, * p < 0.05, ** p < 0.01. (D) RNPEP concentrations in cell supernatant of THLE‐2, MHCC‐97L, HCC‐LM3 and MHCC‐97H. Data were acquired by ELISA, and presented as the mean ± SD, n = 3/group, * p < 0.05, ** p < 0.01, *** p < 0.001.

    Article Snippet: A normal human liver epithelial cell line (THLE‐2) was purchased from Procell Life Science & Technology Co., Ltd. (Wuhan, China) and cultured in cell‐specific culture medium (CM‐0833, Procell Life Science & Technology) at 37°C in a 5% CO 2 in air incubator.

    Techniques: Expressing, Real-time Polymerase Chain Reaction, Enzyme-linked Immunosorbent Assay