Evidence map›Paper›PMID 31355132›Full record

ArticleFrontiers in oncology2019

Human SP-D Acts as an Innate Immune Surveillance Molecule Against Androgen-Responsive and Androgen-Resistant Prostate Cancer Cells.

Gargi Thakur, Gagan Prakash, Vedang Murthy, Nilesh Sable, Santosh Menon, Salman H Alrokayan, Haseeb A Khan, Valarmathy Murugaiah, Ganesh Bakshi, Uday Kishore and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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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

11 authors at 5 institutions in 3 countries.

Gargi ThakurDepartment of Innate Immunity, ICMR-National Institute for Research in Reproductive Health, Mumbai, India.
Gagan PrakashTata Memorial Hospital, Homi Bhabha National Institute, Mumbai, India.
Vedang MurthyTata Memorial Hospital, Homi Bhabha National Institute, Mumbai, India.
Nilesh SableTata Memorial Hospital, Homi Bhabha National Institute, Mumbai, India.
Santosh MenonTata Memorial Hospital, Homi Bhabha National Institute, Mumbai, India.
Salman H AlrokayanDepartment of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.
Haseeb A KhanDepartment of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.
Valarmathy MurugaiahBiosciences, College of Health and Life Sciences, Brunel University London, Uxbridge, United Kingdom.
Ganesh BakshiTata Memorial Hospital, Homi Bhabha National Institute, Mumbai, India.
Uday KishoreBiosciences, College of Health and Life Sciences, Brunel University London, Uxbridge, United Kingdom.
Taruna MadanDepartment of Innate Immunity, ICMR-National Institute for Research in Reproductive Health, Mumbai, India.
Tata Memorial Hospital · INBrunel University of London · GBHomi Bhabha National Institute · INKing Saud University · SANational Institute for Research in Reproductive Health · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Surfactant Protein D (SP-D), a pattern recognition innate immune molecule, has been implicated in the immune surveillance against cancer. A recent report showed an association of decreased SP-D expression in human prostate adenocarcinoma with an increased Gleason score and severity. In the present study, the SP-D expression was evaluated in primary prostate epithelial cells (PrEC) and prostate cancer cell lines. LNCaP, an androgen dependent prostate cancer cell line, exhibited significantly lower mRNA and protein levels of SP-D than PrEC and the androgen independent cell lines (PC3 and DU145). A recombinant fragment of human SP-D, rfhSP-D, showed a dose and time dependent binding to prostate cancer cells via its carbohydrate recognition domain. This study, for the first time, provides evidence of significant and specific cell death of tumor cells in rfhSP-D treated explants as well as primary tumor cells isolated from tissue biopsies of metatstatic prostate cancer patients. Viability of PrEC was not altered by rfhSP-D. Treated LNCaP (p53

Indexed as

apoptosisLNCaP cellsp53pAktpattern recognition receptorPC3 cellsprostate tumor explantsviability

Identifiers

PMID31355132
PMCPMC6637921
OpenAlexW2962541500

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.