Evidence map›Paper›PMID 21596021›Full record

ArticleBiochemical and biophysical research communications2011

TNFα enhances the motility and invasiveness of prostatic cancer cells by stimulating the expression of selective glycosyl- and sulfotransferase genes involved in the synthesis of selectin ligands.

Prakash Radhakrishnan, Vishwanath Chachadi, Ming-Fong Lin, Rakesh Singh, Reiji Kannagi, Pi-Wan Cheng

Abstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 2 pooled it
3.0field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 2 syntheses or guidelines pooled it, 50 citations in OpenAlex.

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  9. Adaptation of the Golgi Apparatus in Cancer Cell Invasion and Metastasis.Frontiers in cell and developmental biology · 2021
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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

6 authors at 2 institutions in 2 countries.

Prakash RadhakrishnanDepartment of Biochemistry and Molecular Biology, College of Medicine, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Vishwanath Chachadi
Ming-Fong Lin
Rakesh Singh
Reiji Kannagi
Pi-Wan Cheng
University of Nebraska Medical Center · USAichi Cancer Center · JP

Funding

SIGNALING IN ANDROGEN REFRACTORY PROSTATE CANCERR01CA088184 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI LIN, MING-FONG · 2000 to 2010
$2.6M
BIOSYNTHESIS OF TRACHEAL MUCOUS GLYCOPROTEINSR01HL048282 · NHLBI · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI CHENG, PI-WAN · 1995 to 2010
$2.2M
Control of Mucin Glycan Branching in Membrane-bound and Secreted MucinsR21HL097238 · NHLBI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI CHENG, PI-WAN · 2009 to 2010
$385k
Biosynthesis of Tracheal Mucous GlycoproteinsR56HL048282 · NHLBI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI CHENG, PI-WAN · 2008 to 2008
$368k
NCI NIH HHS R01 CA088184NCI NIH HHS R01 CA88184NHLBI NIH HHS R01 HL048282NHLBI NIH HHS R01 HL48282NHLBI NIH HHS R21 HL097238NHLBI NIH HHS R21 HL97238NHLBI NIH HHS R56 HL048282
6 · The paper itself

Abstract

Sialyl Lewis x (sLe(x)) plays an important role in cancer metastasis. But, the mechanism for its production in metastatic cancers remains unclear. The objective of current study was to examine the effects of a proinflammatory cytokine on the expression of glycosyltransferase and sulfotransferase genes involved in the synthesis of selectin ligands in a prostate cancer cell line. Androgen-independent human lymph node-derived metastatic prostate cancer cells (C-81 LNCaP), which express functional androgen receptor and mimic the castration-resistant advanced prostate cancer, were used. TNFα treatment of these cells increased their binding to P-, E- and L-selectins, anti-sLe(x) antibody, and anti-6-sulfo-sialyl Lewis x antibody by 12%, 240%, 43%, 248% and 21%, respectively. Also, the expression of C2GnT-1, B4GalT1, GlcNAc6ST3, and ST3Gal3 genes was significantly upregulated. Further treatment of TNFα-treated cells with either anti-sLe(x) antibody or E-selectin significantly suppressed their in vitro migration (81% and 52%, respectively) and invasion (45% and 56%, respectively). Our data indicate that TNFα treatment enhances the motility and invasion properties of LNCaP C-81 cells by increasing the formation of selectin ligands through stimulation of the expression of selective glycosyl- and sulfotransferase genes. These results support the hypothesis that inflammation contributes to cancer metastasis.

Indexed as

Gene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticCell Line, TumorCell MovementE-SelectinGlycosyltransferasesHumansLigandsL-SelectinMaleNeoplasm InvasivenessOligosaccharidesProstatic NeoplasmsP-SelectinSialyl Lewis X AntigenSulfotransferasesE-SelectinGlycosyltransferasesLigandsL-SelectinOligosaccharidesP-SelectinSialyl Lewis X AntigenSulfotransferasesTumor Necrosis Factor-alpha

Identifiers

PMID21596021
PMCPMC4011552
OpenAlexW1986233036

What OpenQuestion holds

Textmetadata
LicenceTDM
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.