Evidence map›Paper›PMID 25715123›Full record

ArticleStem cells and development2015

VAV3 Overexpressed in Cancer Stem Cells Is a Poor Prognostic Indicator in Ovarian Cancer Patients.

Ah-Young Kwon, Gwang-Il Kim, Ju-Yeon Jeong, Ji-Ye Song, Kyu-Beom Kwack, Chan Lee, Hae-Youn Kang, Tae-Heon Kim, Jin-Hyung Heo, Hee Jung An

Open access · greenAbstract read
In one paragraph

Article in Stem cells and development, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 31 citations in OpenAlex.

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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.

Ah-Young Kwon1 Department of Pathology, College of Medicine, CHA University , Sungnam, Republic of Korea.
Gwang-Il Kim1 Department of Pathology, College of Medicine, CHA University , Sungnam, Republic of Korea.
Ju-Yeon Jeong2 Institute for Clinical Research, College of Medicine, CHA University , Sungnam, Republic of Korea.
Ji-Ye Song2 Institute for Clinical Research, College of Medicine, CHA University , Sungnam, Republic of Korea.
Kyu-Beom Kwack3 Department of Biomedical Science, College of Medicine, CHA University , Sungnam, Republic of Korea.
Chan Lee4 Department of Gynecologic Oncology, College of Medicine, CHA University , Sungnam, Republic of Korea.
Hae-Youn Kang1 Department of Pathology, College of Medicine, CHA University , Sungnam, Republic of Korea.
Tae-Heon Kim1 Department of Pathology, College of Medicine, CHA University , Sungnam, Republic of Korea.
Jin-Hyung Heo1 Department of Pathology, College of Medicine, CHA University , Sungnam, Republic of Korea.
Hee Jung An1 Department of Pathology, College of Medicine, CHA University , Sungnam, Republic of Korea.
CHA University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ovarian carcinoma is a highly lethal malignancy due to frequent relapse and drug resistance. Cancer stem cells (CSCs) are thought to contribute significantly to disease relapse and drug resistance. In this study, a subpopulation of CSCs of ovarian carcinoma was isolated and the genes differentially expressed in these cells were identified to characterize CSCs and to find candidate biomarkers. Ovarian carcinoma cells from patients were primarily cultured, and spheroid-forming cells (SFCs) were isolated. The characteristic genes of SFCs were identified through cDNA microarray and validation by quantitative real-time polymerase chain reaction and immunohistochemistry, and the association of their expression with clinicopathologic parameters was analyzed. GSC (4.26-fold), VAV3 (7.05-fold), FOXA2 (12.06-fold), LEF1 (17.26-fold), COMP (21.33-fold), GRIN2A (9.36-fold), CD86 (23.14-fold), PYY (4.18-fold), NKX3-2 (10.35-fold), and PDK4 (74.26-fold) were significantly upregulated in SFCs compared with parental cancer cells. With validation for human ovarian carcinomas, LEF1, PYY, NKX3-2, and WNT3A were significantly upregulated in chemoresistant cancers compared with chemosensitive cancers. Overexpression of LEF1, VAV3, and NKX3-2 was significantly associated with distant metastasis by immunohistochemistry. VAV3 overexpression was an independent poor survival indicator (hazard ratio=15.27, P<0.05) by multivariate Cox analysis. The further functional assay revealed that VAV3 knockdown regulated CSC activation and ovarian cancer cell proliferation and sensitized paclitaxel (PTX)-resistant cancer cells to PTX treatment. Taken together, we identified by high-throughput analysis of CSCs that VAV3 overexpression is a novel biomarker for poor prognosis and survival in ovarian carcinoma.

Indexed as

AgedBiomarkers, TumorCarcinomaFemaleHumansMiddle AgedNeoplastic Stem CellsOvarian NeoplasmsProto-Oncogene Proteins c-vavUp-RegulationBiomarkers, TumorProto-Oncogene Proteins c-vavVAV3 protein, human

Identifiers

PMID25715123
PMCPMC4499777
OpenAlexW2312216396

What OpenQuestion holds

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Registered trials

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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.