Evidence map›Paper›PMID 28559013›Full record

ArticleOral oncology2017

Establishment and genomic characterization of primary salivary duct carcinoma cell line.

Jie Li, Yohitsugu Mitani, Pulivarthi H Rao, Laszlo Perlaky, Bin Liu, Randal S Weber, Adel K El-Naggar

Abstract read
In one paragraph

Article in Oral oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Reciprocal and Autonomous Glucocorticoid and Androgen Receptor Activation in Salivary Duct Carcinoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
    Article
  5. Article
  6. 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

7 authors.

Jie LiThe University of Texas, M.D. Anderson Cancer Center, Department of Pathology, United States.
Yohitsugu MitaniThe University of Texas, M.D. Anderson Cancer Center, Department of Pathology, United States.
Pulivarthi H RaoBaylor College of Medicine, Department of Pediatrics, Texas Children's Cancer and Hematology Centers, United States.
Laszlo PerlakyBaylor College of Medicine, Department of Pediatrics, Texas Children's Cancer and Hematology Centers, United States.
Bin LiuThe University of Texas, M.D. Anderson Cancer Center, Department of Genetics, United States.
Randal S WeberThe University of Texas, M.D. Anderson Cancer Center, Department of Head and Neck Surgery, United States.
Adel K El-NaggarThe University of Texas, M.D. Anderson Cancer Center, Department of Pathology, United States. Electronic address: anaggar@mdanderson.org.

Funding

Targeting the p53 pathway for reversal of oral premalignancyP50CA097007 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MYERS, JEFFREY NICHOLAS · 2002 to 2012
$26.1M
NCI NIH HHS P50 CA097007NIDCR NIH HHS HHSN268200900039C
6 · The paper itself

Abstract

objectivesTo develop and characterize in vitro salivary duct carcinoma as a surrogate for functional studies. MATERIALS AND

methodsCells were dispersed from tumor tissue fragments under sterile conditions in RPMI media. Disassociated cells were cultivated, immortalized with hTERT and propagated for more than 100 passages. Morphologic, linage, cytogenetic and genomic analyses were performed on different passages of cell line and primary tumor. Soft agar growth was performed.

resultsAnalysis of cytomorphologic features, growth characteristics and lineage specific markers expression confirmed the epithelial derivation and the neoplastic nature of the cell line. DNA STRs analysis showed identical match of both cell line and primary tumor. Cultivated cells expressed Androgen Receptor (AR), PTEN, and EFGR proteins and the AR-V7 isoform transcript. Comparative exome-sequencing identified common mutated genes in both cell line and primary tumor. In-vitro colony formation of late passages is established.

conclusionWe report the development of the first human salivary duct carcinoma cell line (MDA-SDC-04) that retains critical biological and genomic features of the donor tumor.

Indexed as

AnimalsCell Line, TumorExomeHeterograftsHumansKaryotypingMiceMicrosatellite RepeatsReverse Transcriptase Polymerase Chain ReactionSalivary DuctsSalivary Gland NeoplasmsAndrogen receptorCell line developmentCell line validationSalivary duct carcinomaSalivary gland carcinomas

Identifiers

PMID28559013
PMCPMC5531198

What OpenQuestion holds

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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.