Evidence map›Paper›PMID 31064850›Full record

ArticleCancer research2019

Upregulation of Scavenger Receptor B1 Is Required for Steroidogenic and Nonsteroidogenic Cholesterol Metabolism in Prostate Cancer.

Jacob A Gordon, Jake W Noble, Ankur Midha, Fatemeh Derakhshan, Gang Wang, Hans H Adomat, Emma S Tomlinson Guns, Yen-Yi Lin, Shancheng Ren, Collin C Collins and 4 more

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

41 citing papers in PubMed, 65 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

14 authors at 7 institutions in 5 countries.

Jacob A GordonVancouver Prostate Centre, Vancouver Coastal Health Research Institute, Vancouver, Canada.
Jake W NobleVancouver Prostate Centre, Vancouver Coastal Health Research Institute, Vancouver, Canada.
Ankur MidhaInstitute of Immunology, Freie Universität Berlin, Berlin, Germany.
Fatemeh DerakhshanDepartment of Pathology, British Columbia Cancer Agency, Vancouver, Canada.
Gang WangDepartment of Pathology, British Columbia Cancer Agency, Vancouver, Canada.
Hans H AdomatVancouver Prostate Centre, Vancouver Coastal Health Research Institute, Vancouver, Canada.
Emma S Tomlinson GunsVancouver Prostate Centre, Vancouver Coastal Health Research Institute, Vancouver, Canada.
Yen-Yi LinVancouver Prostate Centre, Vancouver Coastal Health Research Institute, Vancouver, Canada.
Shancheng RenDepartment of Urology, Second Military Medical University, Shanghai, China.
Collin C CollinsVancouver Prostate Centre, Vancouver Coastal Health Research Institute, Vancouver, Canada.
Peter S NelsonHuman Biology Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Colm MorrisseyDepartment of Urology, University of Washington, Seattle, Washington.
Kishor M WasanFaculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, Canada.
Michael E CoxVancouver Prostate Centre, Vancouver Coastal Health Research Institute, Vancouver, Canada. mcox@prostatecentre.com.
Vancouver Coastal Health · CABC Cancer Agency · CACape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa · ZAFreie Universität Berlin · DESecond Military Medical University · CNUniversity of British Columbia · CAUniversity of Washington · US

Funding

TRANSCRIPTOME AND PROTEOME STRATIFICATION OF PROSTATE ADENOCARCINOMA PHENOTYPESP50CA097186 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PETER S NELSON · 2002 to 2026
$58.1M
Steroid Metabolism in Castration-Resistant Prostate CancerP01CA163227 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI PETER S NELSON · 2013 to 2026
$25.0M
NCI NIH HHS P01 CA163227NCI NIH HHS P50 CA097186
6 · The paper itself

Abstract

Aberrant cholesterol metabolism is increasingly appreciated to be essential for prostate cancer initiation and progression. Transcript expression of the high-density lipoprotein-cholesterol receptor scavenger receptor B1 (SR-B1) is elevated in primary prostate cancer. Hypothesizing that SR-B1 expression may help facilitate malignant transformation, we document increased SR-B1 protein and transcript expression in prostate cancer relative to normal prostate epithelium that persists in lethal castration-resistant prostate cancer (CRPC) metastasis. As intratumoral steroid synthesis from the precursor cholesterol can drive androgen receptor (AR) pathway activity in CRPC, we screened androgenic benign and cancer cell lines for sensitivity to SR-B1 antagonism. Benign cells were insensitive to SR-B1 antagonism, and cancer line sensitivity inversely correlated with expression levels of full-length and splice variant AR. In androgen-responsive CRPC cell model C4-2, SR-B1 antagonism suppressed cholesterol uptake,

Indexed as

AndrogensAnimalsApoptosisBiomarkers, TumorBone NeoplasmsCell ProliferationCholesterolGene Expression Regulation, NeoplasticHumansLiver NeoplasmsLung NeoplasmsMaleMiceMice, NudeOrchiectomyPrognosisAndrogensAR protein, humanBiomarkers, TumorCholesterolReceptors, AndrogenSCARB1 protein, humanScavenger Receptors, Class B

Identifiers

PMID31064850
PMCPMC6606386
OpenAlexW2944243263

What OpenQuestion holds

Textmetadata
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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.