Evidence map›Paper›PMID 24416385›Full record

ArticlePloS one2014

Establishment and characterization of 7 novel hepatocellular carcinoma cell lines from patient-derived tumor xenografts.

Hong Xin, Ke Wang, Gang Hu, Fubo Xie, Kedong Ouyang, Xuzhen Tang, Minjun Wang, Danyi Wen, Yizhun Zhu, Xiaoran Qin

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 13% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

23 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Review
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  7. Review
  8. Article
  9. Article
  10. Oncology letters · 2018
    Article
  11. Article
  12. Article
  13. Article
  14. GPRC5A: An Emerging Biomarker in Human Cancer.BioMed research international · 2018
    Review
  15. Article
  16. Article
  17. Article
  18. Explant culture of sarcoma patients' tissue.Laboratory investigation; a journal of technical methods and pathology · 2016
    Article
  19. Article
  20. GPRC5A overexpression predicted advanced biological behaviors and poor prognosis in patients with gastric cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    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

10 authors at 1 institution in 1 country.

Hong XinDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, China.
Ke WangShanghai ChemPartner Co., LTD, Shanghai, China.
Gang HuShanghai ChemPartner Co., LTD, Shanghai, China.
Fubo XieShanghai ChemPartner Co., LTD, Shanghai, China.
Kedong OuyangShanghai ChemPartner Co., LTD, Shanghai, China.
Xuzhen TangShanghai ChemPartner Co., LTD, Shanghai, China.
Minjun WangDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, China.
Danyi WenShanghai ChemPartner Co., LTD, Shanghai, China.
Yizhun ZhuDepartment of Pharmacology, School of Pharmacy, Fudan University, Shanghai, China.
Xiaoran QinShanghai ChemPartner Co., LTD, Shanghai, China.
Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a common cancer with poor prognosis worldwide and the molecular mechanism is not well understood. This study aimed to establish a collection of human HCC cell lines from patient-derived xenograft (PDX) models. From the 20 surgical HCC sample collections, 7 tumors were successfully developed in immunodeficient mice and further established 7 novel HCC cell lines (LIXC002, LIXC003, LIXC004, LIXC006, LIXC011, LIXC012 and CPL0903) by primary culture. The characterization of cell lines was defined by morphology, growth kinetics, cell cycle, chromosome analysis, short tandem repeat (STR) analysis, molecular profile, and tumorigenicity. Additionally, response to clinical chemotherapeutics was validated both in vitro and in vivo. STR analysis indicated that all cell lines were unique cells different from known cell lines and free of contamination by bacteria or mycoplasma. The other findings were quite heterogeneous between individual lines. Chromosome aberration could be found in all cell lines. Alpha-fetoprotein was overexpressed only in 3 out of 7 cell lines. 4 cell lines expressed high level of vimentin. Ki67 was strongly stained in all cell lines. mRNA level of retinoic acid induced protein 3 (RAI3) was decreased in all cell lines. The 7 novel cell lines showed variable sensitivity to 8 tested compounds. LIXC011 and CPL0903 possessed multiple drug resistance property. Sorafenib inhibited xenograft tumor growth of LIXC006, but not of LIXC012. Our results indicated that the 7 novel cell lines with low passage maintaining their clinical and pathological characters could be good tools for further exploring the molecular mechanism of HCC and anti-cancer drug screening.

Indexed as

Chromosome AberrationsFounder EffectAnimalsAntineoplastic AgentsCarcinoma, HepatocellularCell CycleCell Line, TumorFemaleGene ExpressionHeterograftsHumansKaryotypingLiver NeoplasmsMaleMiceMice, SCIDAntineoplastic AgentsNeoplasm Proteins

Identifiers

PMID24416385
PMCPMC3887059
OpenAlexW1978032968

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.