Evidence map›Paper›PMID 28454215›Full record

ArticleOncology letters2017

Evaluation of ALDH1 expression in ipsilateral breast cancer recurrence.

Tadahiko Shien, Takehiro Tanaka, Masahiko Tanabe, Yasuhiro Okumura, Norikazu Masuda, Atsushi Yoshida, Nobuyuki Arima, Yoshifumi Komoike, Satoru Tanaka, Takuji Iwase and 5 more

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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

15 authors at 8 institutions in 1 country.

Tadahiko ShienDepartment of Breast and Endocrine Surgery, Okayama University Hospital, Okayama 700-8558, Japan.
Takehiro TanakaDepartment of Pathology, Okayama University Hospital, Okayama 700-8558, Japan.
Masahiko TanabeDivision of Breast Oncology, The Cancer Institute Hospital of The Japanese Foundation for Cancer Research, Tokyo 135-8550, Japan.
Yasuhiro OkumuraDepartment of Breast and Endocrine Surgery, Kumamoto City Hospital, Kumamoto 862-8505, Japan.
Norikazu MasudaDepartment of Surgery, Breast Oncology, National Hospital Organization Osaka National Hospital, Osaka 540-0006, Japan.
Atsushi YoshidaDepartment of Breast Surgery, St. Luke's International Hospital, Tokyo 104-8560, Japan.
Nobuyuki ArimaDepartment of Breast Oncology, Department of Pathology, Kumamoto Shinto General Hospital, Kumamoto 862-8655, Japan.
Yoshifumi KomoikeDepartment of Breast and Endocrine Surgery, Osaka Medical Center for Cancer and Cardiovascular Diseases, Osaka 537-8511, Japan.
Satoru TanakaSection of Breast and Endocrine Surgery, Department of General and Gastroenterological Surgery, Osaka Medical College, Osaka 569-8686, Japan.
Takuji IwaseDivision of Breast Oncology, The Cancer Institute Hospital of The Japanese Foundation for Cancer Research, Tokyo 135-8550, Japan.
Tetsuya TaguchiDepartment of Endocrine and Breast Surgery, Kyoto Prefectural University of Medicine, Kyoto 602-0841, Japan.
Katsuhiko NakatsukasaDepartment of Endocrine and Breast Surgery, Kyoto Prefectural University of Medicine, Kyoto 602-0841, Japan.
Hideo InajiDepartment of Breast and Endocrine Surgery, Osaka Medical Center for Cancer and Cardiovascular Diseases, Osaka 537-8511, Japan.
Makoto IshitobiDepartment of Breast and Endocrine Surgery, Osaka Medical Center for Cancer and Cardiovascular Diseases, Osaka 537-8511, Japan.
Collaborative Study Group of Scientific Research of the Japanese Breast Cancer Society
Osaka Medical Center for Cancer and Cardiovascular Diseases · JPJapanese Foundation For Cancer Research · JPKumamoto City Hospital · JPKyoto Prefectural University · JPOkayama University Hospital · JPOsaka Medical and Pharmaceutical University · JPOsaka National Hospital · JPSt. Luke's International Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aldehyde dehydrogenase 1 (ALDH1) is a cancer stem cell (CSC) marker that is easily evaluable. The expression and clinical significance of ALDH1 in ipsilateral breast tumor recurrence (IBTR) has yet to be investigated. In the present study, the expression profile of ALDH1 and its correlation with prognosis in IBTR tissues was examined. Patients with IBTR from eight institutions were retrospectively enrolled in the study. Immunohistochemistry was used to examine ALDH1 expression patterns in the tissue specimens of primary cancers and IBTRs. ALDH1 expression levels were investigated in 182 IBTR tumors, which included cases of invasive carcinoma selected from 271 consecutive patients with IBTR. ALDH1 was expressed in 23% of the IBTR tissue samples. The rate of concordant expression between primary cancer and IBTR tissues was 68%. There was no significant association between disease-free survival (DFS) and ALDH1 expression levels in IBTR. IBTRs that expressed ALDH1 and Ki-67 had a poorer prognosis and this expression pattern was significantly associated with DFS (P=0.0073). The percentages of ALDH1 positive expression in each tissue subtype were as follows: Luminal A, 20%; luminal B, 24%; human epidermal growth factor 2 (HER2), 35%; triple-negative, 21%. There was a significant correlation between DFS and ALDH1 expression levels in HER2-type IBTR tissue specimens (P=0.034). In conclusion, it is possible that ALDH1 and Ki-67 expression levels may be useful for predicting prognosis in patients with HER2-type tumors.

Indexed as

aldehyde dehydrogenase 1breast cancercancer stem cellipsilateral breast tumor recurrenceprognostic factor

Identifiers

PMID28454215
PMCPMC5403634
OpenAlexW2566894218

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LicenceCC BY-NC-ND
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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.