MDA-7/IL-24 regulates proliferation, invasion and tumor cell radiosensitivity: A new cancer therapy?

被引:21
作者
Dent, P
Yacoub, A
Grant, S
Curiel, DT
Fisher, PB
机构
[1] Virginia Commonwealth Univ, Dept Biochem, Richmond, VA 23298 USA
[2] Virginia Commonwealth Univ, Dept Hematol Oncol, Richmond, VA 23298 USA
[3] Columbia Univ Coll Phys & Surg, Med Ctr, Dept Pathol, New York, NY 10032 USA
[4] Columbia Univ Coll Phys & Surg, Med Ctr, Dept Neurosurg, New York, NY 10032 USA
[5] Columbia Univ Coll Phys & Surg, Med Ctr, Dept Urol, New York, NY 10032 USA
[6] Univ Alabama Birmingham, Gene Therapy Ctr, Birmingham, AL 35294 USA
关键词
radiation; MDA-7; IL-24; kinase; caspase;
D O I
10.1002/jcb.20502
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The novel cytokine MDA-7/IL-24 was identified by subtractive hybridization in the mid-1990s as a cytokine whose expression increased during the induction of terminal differentiation, and that was either not expressed or was present at low levels in tumor cells compared to non-transformed cells. Multiple studies from several laboratories have subsequently demonstrated that expression of IL-24 in tumor cells, but not in non-transformed cells, causes their growth arrest and ultimately cell death. In addition, IL-24 has been noted to be a radiosensitizing cytokine, which in part is due to the generation of reactive oxygen species(ROS) and causing endoplasmic reticulum stress. Recent publications of Phase I trial data have shown that a recombinant adenovirus to express MDA-7/IL-24 (Ad.mda-7(INGN 241)) was safe and had tumoricidal effects in patients, which argues that IL-24 may have therapeutic value. This review describes what is known about the impact of IL-24 on tumor cell biology in addition to approaches that may enhance the toxicity of this novel cytokine. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:712 / 719
页数:8
相关论文
共 52 条
[1]   Identification of a novel Bcl-xL phosphorylation site regulating the sensitivity of taxol- or 2-methoxyestradiol-induced apoptosis [J].
Basu, A ;
Haldar, S .
FEBS LETTERS, 2003, 538 (1-3) :41-47
[2]  
Cartee L, 2000, INT J ONCOL, V16, P413
[3]   The protein product of the tumor suppressor gene, melanoma differentiation-associated gene 7, exhibits immunostimulatory activity and is designated IL-24 [J].
Caudell, EG ;
Mumm, JB ;
Poindexter, N ;
Ekmekcioglu, S ;
Mhashilkar, AM ;
Yang, XHH ;
Retter, MW ;
Hill, P ;
Chada, S ;
Grimm, EA .
JOURNAL OF IMMUNOLOGY, 2002, 168 (12) :6041-6046
[4]   Bystander activity of Ad-mda7: Human MDA-7 protein kills melanoma cells via an IL-20 receptor-dependent but STAT3-independent mechanism [J].
Chada, S ;
Mhashilkar, AM ;
Ramesh, R ;
Mumm, JB ;
Sutton, RB ;
Bocangel, D ;
Zheng, MZ ;
Grimm, EA ;
Ekmekcioglu, S .
MOLECULAR THERAPY, 2004, 10 (06) :1085-1095
[5]   Clinical and local biological effects of an intraturnoral injection of mda-7 (IL24; INGN 241) in patients with advanced carcinoma:: a phase I study [J].
Cunningham, CC ;
Chada, S ;
Merritt, JA ;
Tong, A ;
Senzer, N ;
Zhang, Y ;
Mhashilkar, A ;
Parker, K ;
Vukelja, S ;
Richards, D ;
Hood, J ;
Coffee, K ;
Nemunaitis, J .
MOLECULAR THERAPY, 2005, 11 (01) :149-159
[6]   Radiation-induced release of transforming growth factor α activates the epidermal growth factor receptor and mitogen-activated protein kinase pathway in carcinoma cells, leading to increased proliferation and protection from radiation-induced cell death [J].
Dent, P ;
Reardon, DB ;
Park, JS ;
Bowers, G ;
Logsdon, C ;
Valerie, K ;
Schmidt-Ullrich, R .
MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (08) :2493-2506
[7]   Cutting edge: STAT activation by IL-19, IL-20 and mda-7 through IL-20 receptor complexes of two types [J].
Dumoutier, L ;
Leemans, C ;
Lejeune, D ;
Kotenko, SV ;
Renauld, JC .
JOURNAL OF IMMUNOLOGY, 2001, 167 (07) :3545-3549
[8]   Down-regulated melanoma differentiation associated gene (MDA-7) expression in human melanomas [J].
Ekmekcioglu, S ;
Ellerhorst, J ;
Mhashilkar, AM ;
Sahin, AA ;
Read, CM ;
Prieto, VG ;
Chada, S ;
Grimm, EA .
INTERNATIONAL JOURNAL OF CANCER, 2001, 94 (01) :54-59
[9]   Loss of MDA-7 expression with progression of melanoma [J].
Ellerhorst, JA ;
Prieto, VG ;
Ekmekcioglu, S ;
Broemeling, L ;
Yekell, S ;
Chada, S ;
Grimm, EA .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (04) :1069-1074
[10]   Vinblastine-induced phosphorylation of Bcl-2 and Bcl-XL is mediated by JNK and occurs in parallel with inactivation of the Raf-1/MEK/ERK cascade [J].
Fan, MY ;
Goodwin, M ;
Vu, T ;
Brantley-Finley, C ;
Gaarde, WA ;
Chambers, TC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (39) :29980-29985