Evidence map›Paper›PMID 31688591›Full record

ArticlePancreas

Establishment and Characterization of 10 Human Pancreatic Cancer Cell Lines Including a HER2 Overexpressed Cell Line.

Soon-Chan Kim, Young-Kyoung Shin, Sun-Whe Kim, Ha-Young Seo, Wooil Kwon, Hongbeom Kim, Youngmin Han, Ja-Oh Lee, Jin-Young Jang, Ja-Lok Ku

Open access · greenAbstract read
In one paragraph

Article in Pancreas. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Modeling pancreatic cancer in mice for experimental therapeutics.Biochimica et biophysica acta. Reviews on cancer · 2021
    Review
  3. Article
  4. 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 2 institutions in 1 country.

Soon-Chan KimFrom the Korean Cell Line Bank, Laboratory of Cell Biology, Cancer Research Institute.
Young-Kyoung ShinFrom the Korean Cell Line Bank, Laboratory of Cell Biology, Cancer Research Institute.
Sun-Whe KimCancer Research Institute.
Ha-Young SeoFrom the Korean Cell Line Bank, Laboratory of Cell Biology, Cancer Research Institute.
Wooil KwonCancer Research Institute.
Hongbeom KimCancer Research Institute.
Youngmin HanCancer Research Institute.
Ja-Oh LeeFrom the Korean Cell Line Bank, Laboratory of Cell Biology, Cancer Research Institute.
Jin-Young JangCancer Research Institute.
Ja-Lok KuFrom the Korean Cell Line Bank, Laboratory of Cell Biology, Cancer Research Institute.
Seoul National University · KRSeoul National University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe incidence of pancreatic adenocarcinoma (PA) approximates its prevalence, as the malignancy is almost consistently fatal within a year. Although the currently available adjuvant therapy seems to provide survival benefit, it is only moderate, and the standard regimen has not yet been established. Therefore, more biological resources to investigate the PA are needed.

methodsHere, we established and characterized 10 human pancreatic cancer cell lines derived from primary tumor mass. Whole exome sequencing technique was used to identify driver mutations and aberrant pathways in each cell line.

resultsFive anticancer drugs were treated to find half maximal effective concentration (EC50), and the response was analyzed in reference to mutational status. Frame shift mutations in ARID1A gene and HER2 amplification were mutually related to better response to the anticancer drugs. In contrast, frame shift mutation in MSH6 gene was associated with resistance to anticancer drugs.

conclusionsIn summary, we established 10 pancreatic cancer cell lines and integrated various molecular aberrations and features of pancreatic cancer cells. Our biological resources are expected to contribute to facilitating research on PA.

Indexed as

AdenocarcinomaCell Line, TumorErb-b2 Receptor Tyrosine KinasesExome SequencingGene AmplificationHumansMutationPancreatic NeoplasmsERBB2 protein, humanErb-b2 Receptor Tyrosine Kinases

Identifiers

PMID31688591
PMCPMC6867661
OpenAlexW2986137804

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.