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STAT3: A Novel Molecular Mediator of Resistance to Chemoradiotherapy
被引:78
|作者:
Spitzner, Melanie
[1
]
Ebner, Reinhard
[2
]
Wolff, Hendrik A.
[3
]
Ghadimi, B. Michael
[1
]
Wienands, Juergen
[4
]
Grade, Marian
[1
]
机构:
[1] Univ Med Gottingen, Dept Gen Visceral & Pediat Surg, Robert Koch Str 40, D-37075 Gottingen, Germany
[2] NCI, Genet Branch, NIH, Bethesda, MD 20892 USA
[3] Univ Med Gottingen, Dept Radiotherapy & Radiooncol, D-37075 Gottingen, Germany
[4] Univ Med Gottingen, Dept Cellular & Mol Immunol, D-37073 Gottingen, Germany
来源:
CANCERS
|
2014年
/
6卷
/
04期
关键词:
STAT3;
cancer;
radiotherapy;
chemoradiotherapy;
chemoradiotherapy-resistance;
chemoradiotherapy-sensitization;
molecular target;
SQUAMOUS-CELL CARCINOMA;
RADIATION-INDUCED APOPTOSIS;
LUNG-CANCER CELLS;
ANAPLASTIC THYROID-CARCINOMA;
LOCALIZED PROSTATE-CANCER;
INVASIVE BLADDER-CANCER;
SIGNAL TRANSDUCER;
CONSTITUTIVE ACTIVATION;
TRANSCRIPTION;
ENHANCES RADIOSENSITIVITY;
D O I:
10.3390/cancers6041986
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Chemoradiotherapy (CRT) represents a standard treatment for many human cancers, frequently combined with radical surgical resection. However, a considerable percentage of primary cancers are at least partially resistant to CRT, which represents a substantial clinical problem, because it exposes cancer patients to the potential side effects of both irradiation and chemotherapy. It is therefore exceedingly important to determine the molecular characteristics underlying CRT-resistance and to identify novel molecular targets that can be manipulated to re-sensitize resistant tumors to CRT. In this review, we highlight much of the recent evidence suggesting that the signal transducer and activator of transcription 3 (STAT3) plays a prominent role in mediating CRT-resistance, and we outline why inhibition of STAT3 holds great promise for future multimodal treatment concepts in oncology.
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页码:1986 / 2011
页数:26
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