Inflammatory Pathways as Promising Targets to Increase Chemotherapy Response in Bladder Cancer

Joint Authors

Zhu, Zhaowei
Shen, Zhoujun
Xu, Chen

Source

Mediators of Inflammation

Issue

Vol. 2012, Issue 2012 (31 Dec. 2012), pp.1-11, 11 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2012-05-31

Country of Publication

Egypt

No. of Pages

11

Main Subjects

Diseases

Abstract EN

While more and more physicians are choosing chemotherapy for patients with bladder cancer, the current treatment is still far from satisfactory due to low response rate and severe side effects.

Emerging evidence indicates that inflammatory microenvironment is involved in the pathogenesis of bladder cancer.

Recent studies have also provided ample evidence that chemotherapy response is influenced by activation of major inflammatory mediators, including transcription factors, cytokines, chemokines, and COX-2.

We reviewed all published literature addressing the roles of inflammatory microenvironment in bladder cancer and evaluating emerging evidence that inflammatory pathways represent potential therapeutic targets to enhance chemotherapy of bladder cancer.

American Psychological Association (APA)

Zhu, Zhaowei& Shen, Zhoujun& Xu, Chen. 2012. Inflammatory Pathways as Promising Targets to Increase Chemotherapy Response in Bladder Cancer. Mediators of Inflammation،Vol. 2012, no. 2012, pp.1-11.
https://search.emarefa.net/detail/BIM-1001170

Modern Language Association (MLA)

Zhu, Zhaowei…[et al.]. Inflammatory Pathways as Promising Targets to Increase Chemotherapy Response in Bladder Cancer. Mediators of Inflammation No. 2012 (2012), pp.1-11.
https://search.emarefa.net/detail/BIM-1001170

American Medical Association (AMA)

Zhu, Zhaowei& Shen, Zhoujun& Xu, Chen. Inflammatory Pathways as Promising Targets to Increase Chemotherapy Response in Bladder Cancer. Mediators of Inflammation. 2012. Vol. 2012, no. 2012, pp.1-11.
https://search.emarefa.net/detail/BIM-1001170

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-1001170