Evidence map›Paper›PMID 34358244›Full record

ArticlePloS one2021

Connections between prolactin and ovarian cancer.

Amira Alkharusi, Abdullah AlMuslahi, Najwa AlBalushi, Radiya AlAjmi, Sami AlRawahi, Asmaa AlFarqani, Gunnar Norstedt, Fahad Zadjali

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 22 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

8 authors at 2 institutions in 2 countries.

Amira AlkharusiDepartment of Physiology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.ORCID 0000-0002-6671-4431
Abdullah AlMuslahiDepartment of Physiology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
Najwa AlBalushiDepartment of Physiology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
Radiya AlAjmiDepartment of Pathology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
Sami AlRawahiDepartment of Physiology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
Asmaa AlFarqaniDepartment of Physiology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
Gunnar NorstedtDepartment of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
Fahad ZadjaliDepartment of Biochemistry, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.ORCID 0000-0001-5891-4700
Sultan Qaboos University · OMKarolinska Institutet · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ovarian cancer (OC) is characterized by a high morbidity and mortality, highlighting a great need for a better understanding of biological mechanisms that affect OC progression and improving its early detection methods. This study investigates effects of prolactin (PRL) on ovarian cancer cells, analyzes PRL receptors (PRLR) in tissue micro arrays and relates PRLR expression to survival of ovarian cancer. A database, composed of transcript profiles from OC, was searched for PRLR expression and results were put in relation to survival. Expression of PRLR in OC tissue sections and OC cell lines SKOV3, OV2008 and OVSAHO was assessed using immunohistochemistry, western blots and quantitative real-time PCR. The biological function of PRLR was evaluated by proliferation, colony formation and wound healing assays. Levels of PRLR mRNA are related to survival; in epithelial OC a high PRLR mRNA expression is related to a shorter survival. Analysis of a tissue micro array consisting of 84 OC showed that 72% were positive for PRLR immuno-staining. PRLR staining tended to be higher in OC of high grade tumors compared to lower grades. PRLR mRNA and protein can further be detected in OC cell lines. Moreover, in vitro treatment with PRL significantly activated the JAK/STAT pathway. PRLR expression is associated with OC survivals. PRL and its receptor may play an onco-modulatory role and promote tumor aggressiveness in OC. Alternatively, increased PRLR levels may form a base for the development of PRLR antagonist or PRLR antagonist-drug conjugate to increase selective uptake of anti-cancer drugs.

Indexed as

Carcinoma, Ovarian EpithelialCell MovementCell ProliferationFemaleHumansImmunohistochemistryKaplan-Meier EstimateMCF-7 CellsOvarian NeoplasmsPhosphorylationProgression-Free SurvivalProlactinReal-Time Polymerase Chain ReactionReceptors, ProlactinRecombinant ProteinsRNA, MessengerProlactinReceptors, ProlactinRecombinant ProteinsRNA, MessengerSTAT3 protein, humanSTAT3 Transcription FactorSTAT5 Transcription Factor

Identifiers

PMID34358244
PMCPMC8345882
OpenAlexW3190645830

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.