Evidence map›Paper›PMID 36593027›Full record

ArticleIn vivo (Athens, Greece)

Distinct Expression of Surface and Genetic Biomarkers in Prostate Cancer Cell Lines.

Chen-Ying Su, Gwo-Che Huang, I-Cheng Chen, Pei-Yu Chen, Yu-Jen Chen, Hsu-Wei Fang

Open access · diamondAbstract read
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Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

6 authors at 4 institutions in 1 country.

Chen-Ying Su *Department of Chemical Engineering and Biotechnology, National Taipei University of Technology, Taipei, Taiwan, R.O.C.
Gwo-Che Huang *Department of Radiation Oncology, MacKay Memorial Hospital, Taipei, Taiwan, R.O.C.
I-Cheng ChenAccelerator for Happiness and Health Industry, National Taipei University of Technology, Taipei, Taiwan, R.O.C.
Pei-Yu ChenDepartment of Chemical Engineering and Biotechnology, National Taipei University of Technology, Taipei, Taiwan, R.O.C.
Yu-Jen ChenDepartment of Radiation Oncology, MacKay Memorial Hospital, Taipei, Taiwan, R.O.C.
Hsu-Wei FangDepartment of Chemical Engineering and Biotechnology, National Taipei University of Technology, Taipei, Taiwan, R.O.C.; hwfang@ntut.edu.tw.
Mackay Memorial Hospital · TWNational Taipei University of Technology · TWNational Health Research Institutes · TWNational Taipei University of Nursing and Health Science · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimSurface biomarkers, such as CD44 and CD133, have been demonstrated to be expressed in prostate cancer cells, and our previous study has shown that prostate cancer cell lines could be divided into three groups according to the single and combined expression pattern of CD44 and 133. In order to refine prognostication in prostate cancer cells, we further investigated genetic biomarkers, prostate cancer antigen 3 (PCA3), kallikrein 4 (KLK4), and KLK9 in different prostate cancer cell lines. MATERIALS AND

methodsCWR22Rv1, PC3, and DU145 cell lines were cultured until 95% confluence. The single expression of CD44 or CD133 and their combined expression were analyzed by flow cytometry, and gene expression of b-actin, PCA3, KLK4, and KLK9 was analyzed by real-time polymerase chain reaction.

resultsThe single expression of CD133 was less than 4% in all cell lines examined. PC3 and DU145 cells displayed a high expression of CD44 (>91%), whereas CWR22Rv1 was the only cell line that demonstrated a high co-expression of both CD44 and CD133 (>91%). In addition, PC3 and DU145 displayed low expression of PCA3, KLK4, and KLK9 when compared with their own b-actin expression. In contrast, CWR22Rva showed high expression of PCA3 and KLK4 although KLK9 expression was also low.

conclusionBoth surface and genetic biomarkers should be validated for a more accurate prognosis in prostate cancer.

Indexed as

ActinsProstatic NeoplasmsBiomarkers, TumorCell LineHumansMaleProstateActinsBiomarkers, TumorCD133CD44genetic biomarkerKLK4KLK9PCA3prostate cancerSurface biomarker

Identifiers

PMID36593027
PMCPMC9843794
OpenAlexW4313475253

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.