Immunohistochemistry versus PCR Technology for Molecular Subtyping of Breast Cancer: Multicentered Expereinces from Addis Ababa, Ethiopia.

Breast cancer Immunohistochemistry Molecular subtypes Reverse transcription polymerase chain reaction

Journal

Journal of cancer prevention
ISSN: 2288-3649
Titre abrégé: J Cancer Prev
Pays: Korea (South)
ID NLM: 101615965

Informations de publication

Date de publication:
30 Jun 2023
Historique:
received: 28 01 2023
revised: 25 04 2023
accepted: 26 04 2023
medline: 12 7 2023
pubmed: 12 7 2023
entrez: 12 7 2023
Statut: ppublish

Résumé

The application of immunohistochemistry (IHC) for molecular characterization of breast cancer (BC) is of paramount importance; however, it is not universally standardized, subject to observer variability and quantifying is a challenge. An alternative molecular technology, such as endpoint reverse transcription (RT)-PCR gene expression analysis, may improve observer variability and diagnostic accuracy. This study was intended to compare IHC with the RT-PCR based technique and assess the potential of RT-PCR for molecular subtyping of BC. In this comparative cross-sectional study, 54 BC tissues were collected from three public hospitals in Addis Ababa and shipped to Gynaecology department at Martin-Luther University (Germany) for laboratory analysis. Only 41 samples were qualified for IHC and RT-PCR investigation of estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2), and Ki-67 protein expression analysis. Kappa statistics was used to assess the concordance between the two techniques. The overall percent agreement between RT-PCR and IHC was 68.3% for ER (positive percent agreement [PPA] 71.1%; negative percent agreement [NPA] 33.3%), 39.0% for PR (PPA 14.3%; NPA 92.3%), and 82.9% for HER2 (PPA 62.5%; NPA 87.9%). Cohen's κ-values of 0.018 (< 0.20), 0.045 (< 0.200), and 0.481 (0.41-0.60) were generated for ER, PR, and HER2, respectively. Concordance for molecular subtypes was only 56.1% (23/41) and 0.20 kappa value. IHC and endpoint RT-PCR techniques have shown to be discordant for 43% samples. Molecular subtyping using endpoint RT-PCR was fairly concordant with IHC. Thus, endpoint RT-PCR may give an objective result, and can be applied for BC subtyping.

Identifiants

pubmed: 37434799
doi: 10.15430/JCP.2023.28.2.64
pii: jcp-28-2-64
pmc: PMC10331035
doi:

Types de publication

Journal Article

Langues

eng

Pagination

64-74

Informations de copyright

Copyright © 2023 Korean Society of Cancer Prevention.

Déclaration de conflit d'intérêts

CONFLICTS OF INTEREST No potential conflicts of interest were disclosed.

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Auteurs

Dessiet Oma (D)

Department of Medical Biochemistry, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.

Maria Teklemariam (M)

Department of Medical Biochemistry, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.

Daniel Seifu (D)

Department of Biochemistry, University of Global Health Equity, Kigali, Rwanda.

Zelalem Desalegn (Z)

Department of Microbiology, Immunology, and Parasitology, School of Medicine, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.

Endale Anberbir (E)

Department of Surgery, School of Medicine, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.

Tamrat Abebe (T)

Department of Microbiology, Immunology, and Parasitology, School of Medicine, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.

Solomon Mequannent (S)

Department of Pharmacology, School of Pharmacy, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.

Solomon Tebeje (S)

Department of Medical Biochemistry, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.

Wajana Lako Labisso (WL)

Department of Pathology, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.

Classifications MeSH