Evidence map›Paper›PMID 26894602›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

New insight on the biological role of p53 protein as a tumor suppressor: re-evaluation of its clinical significance in triple-negative breast cancer.

Min-Sun Jin, In Ae Park, Ji Young Kim, Yul Ri Chung, Seock-Ah Im, Kyung-Hun Lee, Hyeong-Gon Moon, Wonshik Han, Dong-Young Noh, Han Suk Ryu

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Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Min-Sun JinDepartment of Pathology, Bucheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Bucheon, Gyeonggi-do, Korea.
In Ae ParkDepartment of Pathology, Seoul National University Hospital, Seoul, Korea.
Ji Young KimDepartment of Pathology, Seoul National University Hospital, Seoul, Korea.
Yul Ri ChungDepartment of Pathology, Seoul National University Hospital, Seoul, Korea.
Seock-Ah ImDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Kyung-Hun LeeDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
Hyeong-Gon MoonDepartment of Surgery, Seoul National University Hospital, Seoul, Korea.
Wonshik HanDepartment of Surgery, Seoul National University Hospital, Seoul, Korea.
Dong-Young NohDepartment of Surgery, Seoul National University Hospital, Seoul, Korea.
Han Suk RyuDepartment of Pathology, Seoul National University Hospital, Seoul, Korea. karlnash@naver.com.
Seoul National University Hospital · KRCatholic University of Korea · KRSeoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While p53 mutation is found in the majority of triple-negative breast cancer (TNBC) and despite recent developments in p53-targeting agents, their therapeutic application is still limited by the absence of standard biomarkers and ambiguousness of its essential biological role in cancer. Whole sections from 305 TNBC cases were stained for p53 to determine the correlation with lymph node metastasis and clinical outcomes in the whole cohort as well as in stratified patient groups according to AJCC stage and the use of adjuvant chemotherapy. Reduced immunohistochemical expression of p53 was an independent risk factor for lymph node metastasis. p53 overexpression was predictive of better clinical outcome in all patients (P = 0.012, disease-free survival and P = 0.008, overall survival) and the stratified cohorts of those who had early breast cancer and received adjuvant chemotherapy. Suppression of endogenous mutant p53 by siRNA and induction of wild-type p53 repressed TNBC cell invasion in vitro. In TNBC, increased immunohistochemical expression of p53 may reflect the accumulation of wild-type p53 rather than the mutant form. Strong p53 protein expression may serve as a favorable prognostic indicator and provide evidence for the use of specific agents targeting p53.

Indexed as

AdultAgedBiomarkers, TumorBlotting, WesternDisease-Free SurvivalFemaleGene Knockdown TechniquesHumansImmunohistochemistryKaplan-Meier EstimateMiddle AgedPrognosisProportional Hazards ModelsTriple Negative Breast NeoplasmsTumor Suppressor Protein p53Biomarkers, TumorTP53 protein, humanTumor Suppressor Protein p53ImmunohistochemistryLymph node metastasisP53Triple-negative breast cancerTumor suppressive

Identifiers

PMID26894602
OpenAlexW2284408622

What OpenQuestion holds

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Read underepoch 390

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.