Evidence map›Paper›PMID 20831839›Full record

ArticleWorld journal of surgical oncology2010

Androgen receptor status predicts response to chemotherapy, not risk of breast cancer in Indian women.

Chintamani, Pranjal Kulshreshtha, Anurupa Chakraborty, Lc Singh, Ashwani K Mishra, Dinesh Bhatnagar, Sunita Saxena

Abstract readComparative Study
In one paragraph

Article in World journal of surgical oncology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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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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

7 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

ChintamaniDepartment of Surgery, Indian Council Of Medical Research, New Delhi, India. chintamani7@rediffmail.com
Pranjal Kulshreshtha
Anurupa Chakraborty
Lc Singh
Ashwani K Mishra
Dinesh Bhatnagar
Sunita Saxena

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundConsiderably little is known about the biological role and clinical significance of androgen receptor expression in breast cancer. The objectives of this study were to characterize AR-CAG repeat genotypes in a cohort of women with breast cancer and to determine the influence of AR on response to neoadjuvant chemotherapy and clinical outcome. MATERIALS AND

methodsGenotyping of the AR CAG repeat region was done on 70 patients and 80 healthy aged- matched female controls. To assess response to NACT, tissue samples from 30 LABC cases were evaluated quantitatively by real time for AR mRNA expression. The clinical response was correlated with both the pre and post chemotherapy AR expression. The CAG alleles did not show differences between cases and controls when the mean of short, long and average length of both CAG alleles was considered. However, analysis when done defining short allele as CAGn < 20 (AR1) and the long as CAGn ≥ 20 (AR2), risk was found associated with AR2 allele with marginal significance (P = 0.09). Stratification by age of onset, FH, stage, grade ER and AR status failed to reveal any association with breast cancer risk. Genotype carriers with ≥ 20 CAGn showed decrease of AR mRNA expression although significance could not be established (P = 0.47). Tumours in responders had the higher AR mRNA expression levels in pre neo-adjuvant chemotherapy condition (p < 0.02) which got reduced after neoadjuvant chemotherapy and the difference was found to be significant (P = 0.014).

conclusionsAlthough, expansion of the CAGn in the AR gene doesn't show any major effect on breast cancer risk, patients with positive AR expression, pre neoadjuvant chemotherapy, were found to be good responders and a decrease in mRNA level of AR gene related to the chemotherapy-induced apoptosis could serve as an important independent predictor of response to NACT.

Indexed as

Gene Expression Regulation, NeoplasticAdultAntineoplastic AgentsBiomarkers, TumorBreast NeoplasmsChemotherapy, AdjuvantDisease ProgressionFemaleFollow-Up StudiesGenetic Predisposition to DiseaseGenotypeHumansIncidenceIndiaNeoadjuvant TherapyPolymerase Chain ReactionAntineoplastic AgentsAR protein, humanBiomarkers, TumorReceptors, AndrogenRNA, Neoplasm

Identifiers

PMID20831839
PMCPMC2922205

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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.