Evidence map›Paper›PMID 31832016›Full record

ArticleCancer cell international2019

PAX8 expression in high-grade serous ovarian cancer positively regulates attachment to ECM via Integrin β3.

Amata Amy Soriano, Tiziana de Cristofaro, Tina Di Palma, Serena Dotolo, Priyanka Gokulnath, Antonella Izzo, Gaetano Calì, Angelo Facchiano, Mariastella Zannini

Open access · goldAbstract read
In one paragraph

Article in Cancer cell international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

21 citing papers in PubMed, 30 citations in OpenAlex.

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  20. Kelch-like protein 14 promotes proliferation and migration of ovarian cancer cells.International journal of clinical and experimental pathology · 2020
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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 4 institutions in 1 country.

Amata Amy Soriano *1IEOS, Institute of Experimental Endocrinology and Oncology 'G, Salvatore'-National Research Council, Naples, Italy.
Tiziana de Cristofaro *1IEOS, Institute of Experimental Endocrinology and Oncology 'G, Salvatore'-National Research Council, Naples, Italy.
Tina Di Palma1IEOS, Institute of Experimental Endocrinology and Oncology 'G, Salvatore'-National Research Council, Naples, Italy.
Serena Dotolo4ISA, Institute of Food Science-National Research Council, Avellino, Italy.
Priyanka Gokulnath1IEOS, Institute of Experimental Endocrinology and Oncology 'G, Salvatore'-National Research Council, Naples, Italy.
Antonella Izzo2Dpt. of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy.
Gaetano Calì1IEOS, Institute of Experimental Endocrinology and Oncology 'G, Salvatore'-National Research Council, Naples, Italy.
Angelo Facchiano4ISA, Institute of Food Science-National Research Council, Avellino, Italy.
Mariastella Zannini1IEOS, Institute of Experimental Endocrinology and Oncology 'G, Salvatore'-National Research Council, Naples, Italy.ORCID 0000-0002-5740-9769
Institute for Experimental Endocrinology and Oncology · ITInstitute of Food Science · ITCasa Sollievo della Sofferenza · ITFederico II University Hospital · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOvarian cancer is the third most common cause of death among gynecologic malignancies worldwide. Understanding the biology and molecular pathogenesis of ovarian epithelial tumors is key to developing improved prognostic indicators and effective therapies. We aimed to determine the effects of PAX8 expression on the migrative, adhesive and survival capabilities of high-grade serous carcinoma cells.

methodsPAX8 depleted Fallopian tube secretory cells and ovarian cancer cells were generated using short interfering siRNA.

resultsHere, we report that RNAi silencing of PAX8 sensitizes non-adherent cancer cells to

conclusionsOur results demonstrate that PAX8 modulates the interaction of tumor cells with the extracellular matrix (ECM). Notably, we also highlight a novel pathway downstream this transcription factor. Overall, PAX8 could be a potential therapeutic target for high-grade serous carcinoma.

Indexed as

Fallopian tube epithelial secretory cellsIntegrinsIntegrin β3Ovarian cancerPAX8

Identifiers

PMID31832016
PMCPMC6865034
OpenAlexW2991342374

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.