Evidence map›Paper›PMID 25755770›Full record

ArticleInternational journal of clinical and experimental pathology2015

Elevated Aurora B expression contributes to chemoresistance and poor prognosis in breast cancer.

Yiqian Zhang, Chunling Jiang, Huilan Li, Feng Lv, Xiaoyan Li, Xiaolong Qian, Li Fu, Bo Xu, Xiaojing Guo

Abstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
–field-weighted citation impact
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

34 citing papers in PubMed.

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  15. Aurora B kinase: a potential drug target for cancer therapy.Journal of cancer research and clinical oncology · 2021
    Review
  16. Review
  17. Article
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  19. [Aurora kinase-B silencing promotes apoptosis of osteosarcoma 143B cells by ULK1 phosphorylation-induced autophagy].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2020
    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

9 authors.

Yiqian ZhangDepartment of Breast Pathology and Lab, Key Laboratory of Breast Cancer Prevention and Therapy, National Clinical Research Center of Cancer, Tianjin Medical University Cancer Institute and Hospital Tianjin 300060, China.
Chunling JiangDepartment of Oncology, Southern Research Institute Birmingham, AL 35205.
Huilan LiDepartment of Breast Pathology and Lab, Key Laboratory of Breast Cancer Prevention and Therapy, National Clinical Research Center of Cancer, Tianjin Medical University Cancer Institute and Hospital Tianjin 300060, China.
Feng LvDepartment of Breast Pathology and Lab, Key Laboratory of Breast Cancer Prevention and Therapy, National Clinical Research Center of Cancer, Tianjin Medical University Cancer Institute and Hospital Tianjin 300060, China.
Xiaoyan LiDepartment of Breast Pathology and Lab, Key Laboratory of Breast Cancer Prevention and Therapy, National Clinical Research Center of Cancer, Tianjin Medical University Cancer Institute and Hospital Tianjin 300060, China.
Xiaolong QianDepartment of Breast Pathology and Lab, Key Laboratory of Breast Cancer Prevention and Therapy, National Clinical Research Center of Cancer, Tianjin Medical University Cancer Institute and Hospital Tianjin 300060, China.
Li FuDepartment of Breast Pathology and Lab, Key Laboratory of Breast Cancer Prevention and Therapy, National Clinical Research Center of Cancer, Tianjin Medical University Cancer Institute and Hospital Tianjin 300060, China.
Bo XuDepartment of Oncology, Southern Research Institute Birmingham, AL 35205.
Xiaojing GuoDepartment of Breast Pathology and Lab, Key Laboratory of Breast Cancer Prevention and Therapy, National Clinical Research Center of Cancer, Tianjin Medical University Cancer Institute and Hospital Tianjin 300060, China.

Funding

Mechanisms of Mitotic Activation of the ATM kinaseR01CA133093 · NCI · SOUTHERN RESEARCH INSTITUTE · PI XU, BO · 2009 to 2013
$1.4M
NCI NIH HHS R01 CA133093NCI NIH HHS R01CA133-093
6 · The paper itself

Abstract

Aurora-B is a major kinase responsible for appropriate mitotic progression. Elevated expression of Aurora-B has been frequently associated with several types of cancer, including breast cancer. However, it is not clear whether the alteration contributes to tumor responses to therapies and prognosis. In this study, we conducted immunohistochemistry using antibodies against Aurora-B, S1981p-ATM, Ki67, and p53 in paraffin-embedded tumor tissues from 312 invasive breast cancer patients. The correlation between disease-free-survival (DFS) and Aurora-B expression was analyzed using the Kaplan-Meier method and log-rank test. A Cox proportional hazards regression analysis was used to determine whether Aurora-B was an independent prognostic factor for breast cancer. We found that Aurora-B expression was correlated with the proliferation index (P < 0.001) and p53 expression (P = 0.014) in breast cancer tissues. Further we found that Aurora-B expression was associated with lymph node metastasis (P = 0.002) and histological grade (P = 0.001). Multivariate analyses indicated that elevated Aurora-B expression predicted a poor survival. In a subgroup of patients that received neoadjuvant chemotherapy, we found that elevated Aurora-B contributed to chemoresistance (P = 0.011). In conclusion, elevated Aurora-B expression in breast cancer patients contributes to chemoresistance and predicts poor prognosis.

Indexed as

AdultAgedAged, 80 and overAurora Kinase BBiomarkers, TumorBreast NeoplasmsDisease-Free SurvivalDrug Resistance, NeoplasmFemaleHumansImmunohistochemistryKaplan-Meier EstimateMiddle AgedPrognosisProportional Hazards ModelsAURKB protein, humanAurora Kinase BBiomarkers, TumorAurora-Bbreast cancerchemoresistanceprognosis

Identifiers

PMID25755770
PMCPMC4348845

What OpenQuestion holds

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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.