Evidence map›Paper›PMID 24804817›Full record

ArticleJournal of cancer research and clinical oncology2014

Heat shock protein 22 overexpression is associated with the progression and prognosis in gastric cancer.

Xiao-shan Li, Qing Xu, Xiang-yang Fu, Wei-sheng Luo

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Article in Journal of cancer research and clinical oncology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

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21citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

21 citing papers in PubMed.

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  19. The up-regulation of miR-300 in gastric cancer and its effects on cells malignancy.International journal of clinical and experimental medicine · 2015
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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Xiao-shan LiDepartment of Gastroenterology, Affiliated Hospital of Guilin Medical University, 15 Lequn Road, Guilin, 541004, Guangxi Zhuang Autonomous Region, China, lixiaoshan918@126.com.
Qing Xu
Xiang-yang Fu
Wei-sheng Luo

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe heat shock protein 22 (HSP22) is associated with tumor proliferation and protects tumor cell from apoptosis in many malignancies. However, the role of HSP22 in gastric cancer has not been thoroughly elucidated. The aim was to determine the relationship of HSP22 expression with clinicopathological parameters and prognosis in gastric cancer and estimate the alteration of HSP22 expression after neoadjuvant chemotherapy.

methodsHSP22 and matrix metallopeptidase 9 (MMP-9) antigen expressions were evaluated by immunohistochemistry in 129 gastric carcinoma samples. Univariate and multivariate analyses were performed to determine the association between HSP22 expression and prognosis. The response of HSP22 was assessed in 47 patients who received neoadjuvant chemotherapy.

resultsHSP22 protein expression was significantly associated with tumor size, depth invasion, lymph node metastasis and stage of disease (all P < 0.05). In univariate and multivariate analyses, HSP22 was an independent prognostic factor for both overall survival (OS) and recurrence-free survival (RFS) (P = 0.003 and P = 0.004, respectively). Furthermore, HSP22 overexpression was associated with a poor prognosis in all patients and in patients subgroups stratified by tumor size, depth invasion and lymph node metastasis. In addition, HSP22 was significantly correlated with MMP-9 among 129 gastric cancer tissues (P < 0.001). Patients who had MMP-9 overexpression had poor OS and shorter RFS. Moreover, the alteration of HSP22 was not comparable in 47 patients who underwent neoadjuvant chemotherapy.

conclusionsHSP22 plays an important role on tumor aggressiveness and prognosis and may act as a promising target for prognostic prediction.

Indexed as

AdultAgedAged, 80 and overCarcinomaChemotherapy, AdjuvantDisease-Free SurvivalDisease ProgressionFemaleFollow-Up StudiesHeat-Shock ProteinsHumansKaplan-Meier EstimateLymphatic MetastasisMaleMiddle AgedMolecular ChaperonesHeat-Shock ProteinsHSPB8 protein, humanMolecular ChaperonesProtein Serine-Threonine Kinases

Identifiers

PMID24804817
PMCPMC11824078

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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.