Evidence map›Paper›PMID 26486326›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

Establishment and characterization of a human intrahepatic cholangiocarcinoma cell line derived from an Italian patient.

Giuliana Cavalloni, Caterina Peraldo-Neia, Chiara Varamo, Laura Casorzo, Carmine Dell'Aglio, Paola Bernabei, Giovanna Chiorino, Massimo Aglietta, Francesco Leone

Abstract read
In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

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

29 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Leveraging Patient-Derived Organoids for Personalized Liver Cancer Treatment.International journal of biological sciences · 2024
    Article
  5. Review
  6. Article
  7. Human Metastatic Cholangiocarcinoma Patient-Derived Xenografts and Tumoroids for Preclinical Drug Evaluation.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  8. Review
  9. Article
  10. The Curious Case of the HepG2 Cell Line: 40 Years of Expertise.International journal of molecular sciences · 2021
    Review
  11. Patient-Derived Organoids of Cholangiocarcinoma.International journal of molecular sciences · 2021
    Article
  12. Article
  13. Article
  14. Article
  15. Benefits of Zebrafish Xenograft Models in Cancer Research.Frontiers in cell and developmental biology · 2021
    Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Next-Generation Liver Medicine Using Organoid Models.Frontiers in cell and developmental biology · 2019
    Review
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

9 authors.

Giuliana CavalloniMedical Oncology Division, Fondazione del Piemonte per l'Oncologia (FPO), Candiolo Cancer Institute IRCCS, Strada Provinciale 142, Km 3,95, 10060, Candiolo, Turin, Italy. giuliana.cavalloni@ircc.it.
Caterina Peraldo-NeiaMedical Oncology Division, Fondazione del Piemonte per l'Oncologia (FPO), Candiolo Cancer Institute IRCCS, Strada Provinciale 142, Km 3,95, 10060, Candiolo, Turin, Italy.
Chiara VaramoDepartment of Oncology, Candiolo Cancer Institute IRCCS, University of Turin, Strada Provinciale 142, Km 3,95, 10060, Candiolo, Turin, Italy.
Laura CasorzoUnit of Pathology FPO, Candiolo Cancer Institute IRCCS, Strada Provinciale 142, Km 3,95, 10060, Candiolo, Turin, Italy.
Carmine Dell'AglioUnit of Pathology FPO, Candiolo Cancer Institute IRCCS, Strada Provinciale 142, Km 3,95, 10060, Candiolo, Turin, Italy.
Paola BernabeiFlow Cytometry Center, (FPO), Candiolo Cancer Institute IRCCS, Strada Provinciale 142, Km 3,95, 10060, Candiolo, Turin, Italy.
Giovanna ChiorinoCancer Genomics Laboratory, Fondazione Edo ed Elvo Tempia Valenta, Biella, Italy.
Massimo AgliettaMedical Oncology Division, Fondazione del Piemonte per l'Oncologia (FPO), Candiolo Cancer Institute IRCCS, Strada Provinciale 142, Km 3,95, 10060, Candiolo, Turin, Italy.
Francesco LeoneMedical Oncology Division, Fondazione del Piemonte per l'Oncologia (FPO), Candiolo Cancer Institute IRCCS, Strada Provinciale 142, Km 3,95, 10060, Candiolo, Turin, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biliary tract carcinoma is a rare malignancy with multiple causes, which underlie the different genetic and molecular profiles. Cancer cell lines are affordable models, reflecting the characteristics of the tumor of origin. They represent useful tools to identify molecular targets for treatment. Here, we established and characterized from biological, molecular, and genetic point of view, an Italian intrahepatic cholangiocarcinoma cell line (ICC), the MT-CHC01. MT-CHC01 cells were isolated from a tumor-derived xenograft. Immunophenotypical characterization was evaluated both at early and after stabilization passages. In vitro biological, genetic, and molecular features were also investigated. In vivo tumorigenicity was assessed in NOD/SCID mice. MT-CHC01cells retain epithelial cell markers, EPCAM, CK7, and CK19, and some stemness and pluripotency markers, i.e., SOX2, Nanog, CD49f/integrin-α6, CD24, PDX1, FOXA2, and CD133. They grow as a monolayer, with a population double time of about 40 h; they show a low migration and invasion potential. In low attachment conditions, they are able to form spheres and to growth in anchorage-independent manner. After subcutaneous injection, they retain in vivo tumorigenicity; the expression of biliary markers as CA19-9 and CEA were maintained from primary tumor. The karyotype is highly complex, with a hypotriploid to hypertriploid modal number (3n+/-) (52 to 77 chromosomes); low level of HER2 gene amplification, TP53 deletion, gain of AURKA were identified; K-RAS G12D mutation were maintained from primary tumor to MT-CHC01 cells. We established the first ICC cell line derived from an Italian patient. It will help to study either the biology of this tumor or to test drugs both in vitro and in vivo.

Indexed as

AnimalsBile Duct NeoplasmsCarcinogenicity TestsCell Line, TumorCell MovementCholangiocarcinomaComparative Genomic HybridizationDNA Mutational AnalysisFemaleHumansItalyMice, Inbred NODMice, SCIDMiddle AgedMutation, MissenseNeoplasm TransplantationKRAS protein, humanProto-Oncogene Proteins p21(ras)Intrahepatic cholangiocarcinomaIn vitro modelNew cell line

Identifiers

PMID26486326
PMCPMC4844644

What OpenQuestion holds

Textmetadata
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.