Evidence map›Paper›PMID 25337220›Full record

ArticleInternational journal of clinical and experimental pathology2014

Evaluation of BrightGen HR RT-qDx assay to detect nuclear receptors mRNA overexpression in FFPE breast cancer tissue samples for selection of tamoxifen therapy.

Hye-Young Wang, Sangjung Park, Sunghyun Kim, Sungwoo Ahn, Dongsup Lee, Seungil Kim, Dongju Jung, Kwang Hwa Park, Hyeyoung Lee

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. 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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0citing papers 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

The trial behind it

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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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

9 authors at 5 institutions in 1 country.

Hye-Young WangM&D, Inc., Wonju Eco Environmental Technology Center Gangwon, Republic of Korea.
Sangjung ParkDepartment of Biomedical Laboratory Science, College of Health Sciences, Yonsei University Wonju, Gangwon, Republic of Korea ; Department of Clinical Laboratory Science, College of Medical Science, Daegu Haany University Daegu, Republic of Korea.
Sunghyun KimDepartment of Biomedical Laboratory Science, College of Health Sciences, Yonsei University Wonju, Gangwon, Republic of Korea ; Institute for Life Science and Biotechnology, Yonsei University Seoul, Republic of Korea.
Sungwoo AhnDepartment of Biomedical Laboratory Science, College of Health Sciences, Yonsei University Wonju, Gangwon, Republic of Korea.
Dongsup LeeDepartment of Clinical Laboratory Science, Hyejeon College Chungnam, Republic of Korea.
Seungil KimDepartment of Surgery, Yonsei University College of Medicine Seoul, Republic of Korea.
Dongju JungDepartment of Biomedical Laboratory Science, College of Natural Sciences, Hoseo University Chungnam, Republic of Korea.
Kwang Hwa ParkDepartment of Pathology, Wonju College of Medicine, Yonsei University Gangwon, Republic of Korea.
Hyeyoung LeeDepartment of Biomedical Laboratory Science, College of Health Sciences, Yonsei University Wonju, Gangwon, Republic of Korea.
Yonsei University · KRDaegu Haany University · KRHoseo University · KRHyejeon College · KRKorea Institute of Industrial Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is a significant cause of death in women. Estrogen receptor (ER) and progesterone receptor (PR) are important prognostic factors indicating higher recovery rate in the breast cancer patients. Currently, immunohistochemical (IHC) staining is a conventional method to identify expression of ER and PR. If a breast cancer patient expresses ER or PR, a chemotherapy with estrogen inhibitors such as tamoxifen is supposed to be effective. Although IHC staining is a reliable method, it may not a useful method for continuous monitoring of ER and PR expression changes in multiple breast cancer patients. In the present study, we evaluated an alternative method of IHC for detection of ER and PR expression. A quantitative RT-PCR method called 'the BrightGen HR RT-qDx assay' was employed to detect mRNA expression of the nuclear receptors in 199 formalin-fixed paraffin-embedded (FFPE) breast cancer tissue samples. Among the ER/PR positive samples by IHC, 83 were determined positive and 16 were determined negative for the nuclear receptor mRNA by the quantitative RT-PCR method. Among the ER/PR negative samples by IHC, 37 were determined negative and 2 were determined positive by the quantitative RT-PCR method. The overall sensitivity and specificity of the quantitative RT-PCR method were 83.8% and 94.8% (P = 0.0026), respectively. We also optimized the quantitative RT-PCR method by setting up the diagnostic cut-off value using the likelihood ratio. The highest likelihood ratio was when the expression levels of the relative nuclear receptor mRNA passed 103.3 at which sensitivity and specificity was highest. These data suggest that BrightGen HR RT-qDx assay could be an alternative method for detection of the prognostic factors of nuclear receptors expressed in breast cancer patients for providing essential information for therapeutic application of tamoxifen.

Indexed as

FixativesFormaldehydeParaffin EmbeddingReal-Time Polymerase Chain ReactionArea Under CurveBiomarkers, TumorBreast NeoplasmsEstrogen AntagonistsFemaleHumansImmunohistochemistryLikelihood FunctionsMCF-7 CellsPatient SelectionPrecision MedicinePredictive Value of TestsBiomarkers, TumorEstrogen AntagonistsFixativesFormaldehydeReceptors, EstrogenReceptors, ProgesteroneRNA, MessengerTamoxifenBreast cancerERFFPEmolecular diagnosisPRRT-qPCR

Identifiers

PMID25337220
PMCPMC4203191
OpenAlexW333594285

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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.