Evidence map›Paper›PMID 35848881›Full record

ArticleCancer science2022

Polarity switching of ovarian cancer cell clusters via SRC family kinase is involved in the peritoneal dissemination.

Mayuko Kawata, Jumpei Kondo, Kunishige Onuma, Yu Ito, Takeshi Yokoi, Junzo Hamanishi, Masaki Mandai, Tadashi Kimura, Masahiro Inoue

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 14 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

9 authors at 3 institutions in 1 country.

Mayuko KawataDepartment of Clinical Bioresource Research and Development, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Jumpei KondoDepartment of Clinical Bioresource Research and Development, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID https://orcid.org/0000-0002-1350-0480
Kunishige OnumaDepartment of Clinical Bioresource Research and Development, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID https://orcid.org/0000-0002-1034-5796
Yu ItoDepartment of Clinical Bioresource Research and Development, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Takeshi YokoiDepartment of Obstetrics and Gynecology, Kaizuka City Hospital, Kaizuka, Japan.
Junzo HamanishiDepartment of Gynecology and Obstetrics, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID https://orcid.org/0000-0002-7750-0623
Masaki MandaiDepartment of Gynecology and Obstetrics, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Tadashi KimuraDepartment of Obstetrics and Gynecology, Osaka University Graduate School of Medicine, Osaka, Japan.
Masahiro InoueDepartment of Clinical Bioresource Research and Development, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID https://orcid.org/0000-0001-7315-026X
Kyoto University · JPTakarazuka City Hospital · JPThe University of Osaka · JP

Funding

Japan Agency for Medical Research and Development 19cm0106203h0004Japan Agency for Medical Research and Development 21am0401004h0003Japan Society for the Promotion of Science 18H02648Japan Society for the Promotion of Science 21K07942P-CREATEScience and Technology Platform Program for Advanced Biological MedicineTakeda Science Foundation
6 · The paper itself

Abstract

Peritoneal dissemination is a predominant pattern of metastasis in patients with advanced ovarian cancer. Despite recent progress in the management strategy, peritoneal dissemination remains a determinant of poor ovarian cancer prognosis. Using various histological types of patient-derived ovarian cancer organoids, the roles of the apicobasal polarity of ovarian cancer cell clusters in peritoneal dissemination were studied. First, it was found that both ovarian cancer tissues and ovarian organoids showed apicobasal polarity, where zonula occludens-1 (ZO-1) and integrin beta 4 (ITGB4) served as markers for apical and basal sides, respectively. The organoids in suspension culture, as a model of cancer cell cluster floating in ascites, showed apical-out/basal-in polarity status, while once embedded in extracellular matrix (ECM), the organoids switched their polarity to apical-in/basal-out. This polarity switch was accompanied by the SRC kinase family (SFK) phosphorylation and was inhibited by SFK inhibitors. SFK inhibitors abrogated the adherence of the organoids onto the ECM-coated plastic surface. When the organoids were seeded on a mesothelial cell layer, they cleared and invaded mesothelial cells. In vivo, dasatinib, an SFK inhibitor, suppressed peritoneal dissemination of ovarian cancer organoids in immunodeficient mice. These results suggest SFK-mediated polarity switching is involved in peritoneal metastasis. Polarity switching would be a potential therapeutic target for suppressing peritoneal dissemination in ovarian cancer.

Indexed as

Ovarian NeoplasmsAnimalsCarcinoma, Ovarian EpithelialCell Line, TumorDasatinibFemaleHumansIntegrinsMicePlasticssrc-Family KinasesDasatinibIntegrinsPlasticssrc-Family Kinasescell polaritymetastasisorganoidsovarian cancerSRC family kinase

Identifiers

PMID35848881
PMCPMC9530866
OpenAlexW4285730672

What OpenQuestion holds

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LicenceCC BY-NC
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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.