Evidence map›Paper›PMID 26918345›Full record

ArticleOncotarget2016

Markers of fibroblast-rich tumor stroma and perivascular cells in serous ovarian cancer: Inter- and intra-patient heterogeneity and impact on survival.

Sara Corvigno, G Bea A Wisman, Artur Mezheyeuski, Ate G J van der Zee, Hans W Nijman, Elisabeth Åvall-Lundqvist, Arne Östman, Hanna Dahlstrand

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
11.0field-weighted citation impact, top 2% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. PDGFR-βAging · 2021
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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

8 authors at 4 institutions in 2 countries.

Sara CorvignoDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
G Bea A WismanDepartment of Gynecologic Oncology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Artur MezheyeuskiDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Ate G J van der ZeeDepartment of Gynecologic Oncology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Hans W NijmanDepartment of Gynecologic Oncology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Elisabeth Åvall-LundqvistDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Arne ÖstmanDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Hanna DahlstrandDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Karolinska Institutet · SEUniversity Medical Center Groningen · NLKarolinska University Hospital · SELinköping University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inter- and intra-patient variations in tumor microenvironment of serous ovarian cancer are largely unexplored. We aimed to explore potential co-regulation of tumor stroma characteristics, analyze their concordance in primary and metastatic lesions, and study their impact on survival. A tissue microarray (TMA) with 186 tumors and 91 matched metastases was subjected to immunohistochemistry double staining with endothelial cell marker CD34 and fibroblast and pericyte markers α-SMA, PDGFβR and desmin. Images were digitally analyzed to yield "metrics" related to vasculature and stroma features. Intra-case analyses showed that PDGFβR in perivascular cells and fibroblasts were strongly correlated. Similar findings were observed concerning α-SMA. Most stroma characteristics showed large variations in intra-case comparisons of primary tumors and metastasis. Large PDGFβR-positive stroma fraction and high PDGFβFR positive perivascular intensity were both significantly associated with shorter survival in uni- and multi-variate analyses (HR 1.7, 95% CI 1.1-2.5; HR 1.7, 95% CI 1.1-2.8). In conclusion, we found PDGFβR- and α-SMA-expression to be largely independent of each other but concordantly activated in perivascular cells and in fibroblasts within the primary tumor. Stromal characteristics differed between primary tumors and metastases. PDGFβR in perivascular cells and in fibroblasts may be novel prognostic markers in serous ovarian cancer.

Indexed as

AdultAgedAged, 80 and overCystadenocarcinoma, SerousFemaleFibroblastsHumansMiddle AgedOvarian NeoplasmsPericytesPrognosisTumor MicroenvironmentYoung Adultcancer associated fibroblastspericytesprognosisserous ovarian cancertumor microenvironment

Identifiers

PMID26918345
PMCPMC4951310
OpenAlexW2291079623

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.