Evidence map›Paper›PMID 41094661›Full record

ArticleCancer cell international2025

Establishment and characteristic analysis of a novel patient derived cell line of intrahepatic cholangiocarcinoma.

Shuangshuang Dou, Minghui Gao, Quanwei Li, Mengyin Chai, Buxin Kou, Xiaoni Liu

Abstract read
In one paragraph

Article in Cancer cell international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Shuangshuang DouBeijing Institute of Hepatology, Beijing Youan Hospital, Capital Medical University, No.8 Xitoutiao, Youanmenwai, Fengtai District, Beijing, 100069, China.
Minghui GaoBeijing Institute of Hepatology, Beijing Youan Hospital, Capital Medical University, No.8 Xitoutiao, Youanmenwai, Fengtai District, Beijing, 100069, China.
Quanwei LiBeijing Institute of Hepatology, Beijing Youan Hospital, Capital Medical University, No.8 Xitoutiao, Youanmenwai, Fengtai District, Beijing, 100069, China.
Mengyin ChaiBeijing Institute of Hepatology, Beijing Youan Hospital, Capital Medical University, No.8 Xitoutiao, Youanmenwai, Fengtai District, Beijing, 100069, China.
Buxin KouBeijing Institute of Hepatology, Beijing Youan Hospital, Capital Medical University, No.8 Xitoutiao, Youanmenwai, Fengtai District, Beijing, 100069, China.
Xiaoni LiuBeijing Institute of Hepatology, Beijing Youan Hospital, Capital Medical University, No.8 Xitoutiao, Youanmenwai, Fengtai District, Beijing, 100069, China. liuxiaoni888@ccmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIntrahepatic cholangiocarcinoma (ICC) is a primary malignant tumor of the liver, second only to hepatocellular carcinoma. The scarcity of appropriate cell lines has impeded ICC-related research. This study aims to establish a novel patient-derived ICC cell line and systematically evaluate its biological characteristics, thereby providing a valuable cellular tool for ICC research.

methodsA cell line named LPHC-6 of ICC was established using a patient-derived xenograft (PDX) tumor model. We comprehensively characterized this novel cell line through a series of techniques, including cell morphology observation, short tandem repeat (STR) analysis, karyotype analysis, cell proliferation, cell migration assays, western blot analysis, immunofluorescence staining, flow cytometry, gene mutation detection, spheroid formation assays, drug sensitivity testing, and xenograft tumor formation in nude mice.

resultsLPHC-6 cells exhibited typical characteristics of malignant epithelial cells, demonstrating robust proliferation and migration capabilities. These cells possessed a structurally complex triploid karyotype, which was confirmed to be free from cross-contamination with other human cell lines. Tumor biomarker analysis revealed positive expression of AFP and negative expression of GPC3. Additionally, LPHC-6 cells showed high expression levels of stem cell markers CD133 and CD44. The biliary epithelial cell marker CK19 was positive, whereas the hepatocyte marker Hep Par1 was negative. Genomic analysis identified an exon mutation in TP53, copy number loss in PTEN and RAD51, and copy number gain in NTRK1, PDCD1LG2, and VEGFA. Investigations confirmed that LPHC-6 cells exhibited excellent sphere formation ability and tumorigenic potential. Furthermore, LPHC-6 cells demonstrated sensitivity to Sorafenib, Lenvatinib, 5-fluorouracil, Oxaliplatin and Atezolizumab in both 2D and 3D culture system.

conclusionA novel intrahepatic cholangiocarcinoma cell line LPHC-6 has been successfully established, which provides a powerful cell tool for the research related to intrahepatic cholangiocarcinoma.

Indexed as

Biological characteristicsCell lineHuman tumor xenograft modelIntrahepatic cholangiocarcinoma

Identifiers

PMID41094661
PMCPMC12522666

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