Evasion of anti-growth signaling: A key step in tumorigenesis and potential target for treatment and prophylaxis by natural compounds

被引:84
作者
Amin, A. R. M. Ruhul [1 ]
Karpowicz, Phillip A. [2 ]
Carey, Thomas E. [3 ]
Arbiser, Jack [1 ,4 ]
Nahta, Rita [1 ]
Chen, Zhuo G. [1 ]
Dong, Jin-Tang [1 ]
Kucuk, Omer [1 ]
Khan, Gazala N. [5 ]
Huang, Gloria S. [6 ]
Mi, Shijun [6 ]
Lee, Ho-Young [7 ]
Reichrath, Joerg [8 ]
Honoki, Kanya [9 ]
Georgakilas, Alexandros G. [10 ]
Amedei, Amedeo [11 ]
Amin, Amr [12 ,13 ]
Helferich, Bill [14 ]
Boosani, Chandra S. [15 ]
Ciriolo, Maria Rosa [16 ]
Chen, Sophie [17 ]
Mohammed, Sulma I. [18 ]
Azmis, Asfar S. [19 ]
Keith, W. Nicol [20 ]
Bhakta, Dipita [21 ]
Halicka, Dorota [22 ]
Niccolai, Elena
Fujii, Hiromasa [9 ]
Aquilano, Katia [16 ]
Ashraf, S. Salman [12 ]
Nowsheen, Somaira [23 ]
Yang, Xujuan [14 ]
Bilsland, Alan [20 ]
Shin, Dong M. [1 ]
机构
[1] Emory Univ, Winship Canc Inst, Atlanta, GA 30322 USA
[2] Univ Windsor, Dept Biol Sci, Windsor, ON N9B 3P4, Canada
[3] Univ Michigan, Ann Arbor, MI 48109 USA
[4] Atlanta Vet Adm Hlth Ctr, Atlanta, GA USA
[5] Henry Ford Hosp, Detroit, MI 48202 USA
[6] Albert Einstein Coll Med, New York, NY USA
[7] Seoul Natl Univ, Coll Pharm, Seoul, South Korea
[8] Univ Saarland, D-66123 Saarbrucken, Germany
[9] Nara Med Univ, Nara, Japan
[10] Natl Tech Univ Athens, Athens, Greece
[11] Univ Florence, Florence, Italy
[12] UAE Univ, Al Ain, U Arab Emirates
[13] Cairo Univ, Fac Sci, Cairo, Egypt
[14] Univ Illinois, Urbana, IL 61801 USA
[15] Creighton Univ, Omaha, NE 68178 USA
[16] Univ Roma Tor Vergata, Rome, Italy
[17] Ovarian & Prostate Canc Res Lab, Guildford, Surrey, England
[18] Purdue Univ, W Lafayette, IN 47907 USA
[19] Wayne State Univ, Detroit, MI USA
[20] Univ Glasgow, Glasgow, Lanark, Scotland
[21] SASTRA Univ, Sch Chem & Bio Technol, Thanjavur, India
[22] New York Med Coll, Valhalla, NY 10595 USA
[23] Mayo Clin, Mayo Grad Sch, Mayo Med Sch, Med Scientist Training Program, Rochester, MN USA
关键词
Tumor suppressor; Anti-growth signaling; Reversible and irreversible evasion; Cancer prevention; Hallmark of cancer; FACTOR-I RECEPTOR; MACROPHAGE-INHIBITORY CYTOKINE-1; KRUPPEL-LIKE FACTOR-5; BREAST-CANCER CELLS; TUMOR-SUPPRESSOR GENE; FACTOR-BINDING PROTEIN-3; GREEN TEA POLYPHENOL; DIFFERENTIATION FACTOR 15; FACTOR-KAPPA-B; CELLULAR SENESCENCE EVASION;
D O I
10.1016/j.semcancer.2015.02.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The evasion of anti-growth signaling is an important characteristic of cancer cells. In order to continue to proliferate, cancer cells must somehow uncouple themselves from the many signals that exist to slow down cell growth. Here, we define the anti-growth signaling process, and review several important pathways involved in growth signaling: p53, phosphatase and tensin homolog (PTEN), retinoblastoma protein (Rb), Hippo, growth differentiation factor 15 (GDF15), AT-rich interactive domain 1A (ARID1A), Notch, insulin-like growth factor (IGF), and Krfippel-like factor 5 (KLF5) pathways. Aberrations in these processes in cancer cells involve mutations and thus the suppression of genes that prevent growth, as well as mutation and activation of genes involved in driving cell growth. Using these pathways as examples, we prioritize molecular targets that might be leveraged to promote anti-growth signaling in cancer cells. Interestingly, naturally occurring phytochemicals found in human diets (either singly or as mixtures) may promote anti-growth signaling, and do so without the potentially adverse effects associated with synthetic chemicals. We review examples of naturally occurring phytochemicals that may be applied to prevent cancer by antagonizing growth signaling, and propose one phytochemical for each pathway. These are: epigallocatechin-3-gallate (EGCG) for the Rb pathway, luteolin for p53, curcumin for PTEN, porphyrins for Hippo, genistein for GDF15, resveratrol for ARID1A, withaferin A for Notch and diguelin for the IGF1-receptor pathway. The coordination of anti-growth signaling and natural compound studies will provide insight into the future application of these compounds in the clinical setting. (C) 2015 Elsevier Ltd.
引用
收藏
页码:S55 / S77
页数:23
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