Evidence map›Paper›PMID 26551005›Full record

ArticlePloS one2015

Clinical Implications of TβRII Expression in Breast Cancer.

Ningning Gao, Qixi Zhai, Yinyan Li, Kun Huang, Donglin Bian, Xuemei Wang, Caigang Liu, Hong Xu, Teng Zhang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Phase I Trial of M7824 (MSB0011359C), a Bifunctional Fusion Protein Targeting PD-L1 and TGFβ, in Advanced Solid Tumors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
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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

9 authors at 4 institutions in 1 country.

Ningning GaoUltrasonic Diagnosis Department, First Hospital of China Medical University, Shenyang, Liaoning Province, China.
Qixi ZhaiUltrasonic Diagnosis Department, First Hospital of China Medical University, Shenyang, Liaoning Province, China.
Yinyan LiUltrasonic Diagnosis Department, First Hospital of China Medical University, Shenyang, Liaoning Province, China.
Kun HuangUltrasonic Diagnosis Department, First Hospital of China Medical University, Shenyang, Liaoning Province, China.
Donglin BianUltrasonic Diagnosis Department, First Hospital of China Medical University, Shenyang, Liaoning Province, China.
Xuemei WangUltrasonic Diagnosis Department, First Hospital of China Medical University, Shenyang, Liaoning Province, China.
Caigang LiuDepartment of Breast Surgery, Second Hospital of Dalian Medical University, Dalian, Liaoning Province, China.
Hong XuDepartment of Breast Surgery, Liaoning Province Cancer Hospital and Institute, Shenyang, Liaoning Province, China.
Teng ZhangDepartment of Breast Surgery, Liaoning Province Cancer Hospital and Institute, Shenyang, Liaoning Province, China.
First Hospital of China Medical University · CNChina Medical University · CNLiaoning Cancer Hospital & Institute · CNSecond Affiliated Hospital of Dalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo explore the relationship between TβRII [type II TGFβ (transforming growth factor β) receptor] expression and clinicopathological characteristics, and to evaluate the prognostic significance of TβRII expression in breast cancer.

methodsClinicopathological data and prognostic information of 108 patients with histologically confirmed breast cancer who were surgically treated at China Medical University between January 2007 and September 2008 were reviewed and the association between the clinicopathological characteristics and TβRII expression was analyzed by chi-square test and multivariate analysis. The expression of TβRII was assessed by immunohistochemistry.

resultsOf the 108 patients, 60 cases were TβRII positive and 48 cases were negative. There was no significant association between TβRII expression of the patients older than 40 years and that of the younger than 40 years (56.0% vs 50.0%; P = 0.742). The TβRII expression rate was significantly increased in patients with lymph node metastasis compared to those without lymph node metastasis (67.40% vs 46.8%; P = 0.033). Statistically significant relationships were found between increasing tumor clinical stage and high TβRII expression (P = 0.011). TβRII expression was not associated with the expression of ER(estrogen receptor), PR, (progesterone receptor), Her-2 (human epidermal growth factor receptor 2) (P = 0.925,P = 0.861, and P = 0.840, respectively). Patients with high TβRII expression showed poorer 5-year disease-free survival (DFS) compared to those with low expression (66.7% vs 45.6%; P = 0.028) by univariate analysis. Survival analysis demonstrated that TβRII was associated with poor DFS (P = 0.011). Subgroup analysis revealed that TβRII expression was associated with shorter DFS in patients with lymph node metastasis, ER-positive, PR-positive or Her-2-negative tumors (P = 0.006, P = 0.016, P = 0.022, and P = 0.033, respectively). Cox regression analysis revealed that high TβRII expression was related to poor 5-year DFS, and it was an independent factor for predicting the poor outcome for breast cancer patients (P = 0.016).

conclusionsHigh levels of TβRII expression were associated with lymph node metastasis, increasing tumor clinical stage, and poorer 5-year DFS in patients with breast cancer. TβRII may be a potential prognostic marker for breast cancer.

Indexed as

AdultAgedBiomarkers, TumorBreast NeoplasmsDisease-Free SurvivalErb-b2 Receptor Tyrosine KinasesFemaleHumansLymphatic MetastasisMiddle AgedProtein Serine-Threonine KinasesReceptors, EstrogenReceptors, ProgesteroneReceptors, Transforming Growth Factor betaReceptor, Transforming Growth Factor-beta Type IIRetrospective StudiesBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesProtein Serine-Threonine KinasesReceptors, EstrogenReceptors, ProgesteroneReceptors, Transforming Growth Factor betaReceptor, Transforming Growth Factor-beta Type II

Identifiers

PMID26551005
PMCPMC4638357
OpenAlexW2101267614

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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.