Evidence map›Paper›PMID 19659610›Full record

ArticleCancer science2009

Predictors of response to exemestane as primary endocrine therapy in estrogen receptor-positive breast cancer.

Hiroko Yamashita, Satoru Takahashi, Yukashi Ito, Toshinari Yamashita, Yoshiaki Ando, Tatsuya Toyama, Hiroshi Sugiura, Nobuyasu Yoshimoto, Shunzo Kobayashi, Yoshitaka Fujii and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer science, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

22 citing papers in PubMed, 51 citations in OpenAlex.

  1. Trial
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  8. Article
  9. STAT signaling in different breast cancer sub-types.Molecular and cellular endocrinology · 2014
    Review
  10. Article
  11. Article
  12. The role of AIB1 in breast cancer.Oncology letters · 2012
    Article
  13. Review
  14. Review
  15. The Role of Androgen Receptor in Breast Cancer.Drug discovery today. Disease mechanisms · 2012
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

11 authors at 6 institutions in 3 countries.

Hiroko YamashitaOncology, Immunology, and Surgery, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan. hirokoy@med.nagoya-cu.ac.jp
Satoru Takahashi
Yukashi Ito
Toshinari Yamashita
Yoshiaki Ando
Tatsuya Toyama
Hiroshi Sugiura
Nobuyasu Yoshimoto
Shunzo Kobayashi
Yoshitaka Fujii
Hirotaka Iwase
Bipar · FRAichi Cancer Center · JPNagoya City University · JPHigashi Osaka City General Hospital · JPInstitute of Immunology · HRKumamoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endocrine therapy is the most important treatment of choice for estrogen receptor (ER)-positive breast cancer. Potential mechanisms for resistance to endocrine therapy involve ER-coregulatory proteins and cross-talk between ER and other growth factor-signaling networks. However, the factors and pathways responsible for endocrine therapy resistance, particularly resistance to aromatase inhibitors, have not been clearly established. Sixteen postmenopausal patients with ERalpha-positive primary breast cancer were treated daily with 25 mg of exemestane (an aromatase inhibitor) for 6 months. Expressions of ERalpha, ERbeta, progesterone receptor (PgR), androgen receptor (AR), amplified in breast cancer 1 (AIB1), aromatase, epidermal growth factor receptor, human epidermal growth factor receptor type 2, Ki67, cyclin D1, p53, Bcl2, signal transducer and activator of transcription 5 (Stat5), and insulin-like growth factor binding protein 5 (IGFBP5), and phosphorylations of ERalpha serine (Ser) 118, ERalpha Ser167, Akt Ser473, and p44/42 MAPK threonine (Thr) 202/tyrosine (Tyr) 204, were examined by immunohistochemistry on pretreatment tumor biopsies and post-treatment surgical specimens. Analyses were made to test for correlations with response to exemestane. Of the 16 patients, seven responded and nine retained stable disease. High-level expression of AIB1 and phosphorylation of Akt Ser473 were significantly associated with a better response to exemestane, suggesting that these factors could be considered as predictors of exemestane response. Expressions of ERalpha, ERbeta, PgR, aromatase, Ki67, cyclin D1, and p53, and phosphorylations of ERalpha Ser118, ERalpha Ser167, and p44/42 MAPK Thr202/Tyr204, were decreased, whereas expressions of Stat5 and IGFBP5 were increased in post-treatment specimens compared to the values in pretreatment biopsies. Thus, the analysis of factors involved in the estrogen-dependent growth-signaling pathways may be useful in identifying patients responsive to exemestane.

Indexed as

AgedAged, 80 and overAndrostadienesAromatase InhibitorsBreast NeoplasmsEstrogen Receptor alphaEstrogen Receptor betaFemaleHistone AcetyltransferasesHumansImmunohistochemistryKi-67 AntigenNuclear Receptor Coactivator 3PhosphorylationReceptors, EstrogenReceptors, ProgesteroneAndrostadienesAromatase InhibitorsESR1 protein, humanEstrogen Receptor alphaEstrogen Receptor betaexemestaneHistone AcetyltransferasesKi-67 AntigenNCOA3 protein, humanNuclear Receptor Coactivator 3Receptors, EstrogenReceptors, ProgesteroneTrans-Activators

Identifiers

PMID19659610
PMCPMC11158316
OpenAlexW2060378662

What OpenQuestion holds

Textmetadata
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.