The Role of Gender-specific Cytokine Pathways as Drug Targets and Gender-specific Biomarkers in Personalized Cancer Therapy

被引:5
作者
Berghella, Anna Maria [1 ]
Contasta, Ida [1 ]
Lattanzio, Roberto [2 ]
Di Gregorio, Giancarlo [3 ]
Campitelli, Irma [4 ]
Silvino, Marino [5 ]
Liberatore, Luigi Liborio [2 ]
Navarra, Luca [2 ]
Caterino, Giampaolo [2 ]
Mongelli, Antonio [2 ]
Vittorini, Vincenzo [2 ]
Basta, Matteo [3 ]
Domenicucci, Mauro [3 ]
Antonucci, Nunzia [2 ]
Del Beato, Tiziana [1 ]
Secinaro, Enzo [6 ]
Ciccone, Fabiana [7 ]
Pellegrini, Patrizia [1 ]
机构
[1] CNR, IFT, UOS, Laquila, Italy
[2] Osped SS Trinita, Dipartimento Chirurg Gen, Popoli, PE, Italy
[3] Osped SS Trinita, Lab Anal Clin, Popoli, PE, Italy
[4] Osped S Spirito, UOC Microbiol & Virol Clin, Pescara, Italy
[5] Osped SS Trinita, Ctr Trasfus, Popoli, PE, Italy
[6] Univ G DAnnunzio Chieti, Fac Med, Pescara, Italy
[7] Osped S Salvatore, Dipartimento Gastroenterol, Laquila, Italy
关键词
Personalized therapy; tumor treatment; drug targets and biomarkers; cytokine physiological network; gender-specific cytokine pathways; GROWTH-FACTOR-BETA; T-CELLS; COLORECTAL-CANCER; COLON-CANCER; IMMUNE-RESPONSE; TGF-BETA; MULTIPLE-SCLEROSIS; PERIPHERAL-BLOOD; IMMUNOLOGICAL IMPLICATIONS; ADJUVANT CHEMOTHERAPY;
D O I
10.2174/1389450117666160630173647
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The definition of personalized treatments in tumor disease could lead to an improvement of the therapeutic success rate. Therefore, biomarkers are urgently required in order to select the patients that could benefit from adjuvant therapies in the initial phase of the disease and to better define and treat the clinical/therapeutic subgroups in the advanced pathological phases. Disregulation of cytokine physiological network is directly involved in the genesis and progression of tumors. Cytokines are of central importance in the regulation of immune system, but they are rarely released singly: each cyto-kine is able to induce the production of many other factors leading to a network in which they cooperate with other cell regulators such as hormones and neuropeptides. For these reasons the research must be directed to the evaluation of the interrelationships between the different cytokines and their respective pathways, as well as their contribution to the disease aetiology and progression in order to identify real and effective drug targets and biomarkers. The T CD4+ helper cells (Th) have various subpopulations, among which Th1, Th2, Th3, Th9 and Th17, respectively produce cytokines. It has become clear that disorders within the interactions of the network of these cytokines can produce neoplastic diseases. Fur-thermore, studies focusing on gender have shown that the homeostasis of the immune system is con-trolled by pathways of cytokines that are different between sexes and defined for this reason " genderspecifics". Therefore, this perspective article aims to highlight the significance of these cytokine path-ways in order to identify new clinical strategies and personalized therapy in neoplastic diseases.
引用
收藏
页码:485 / 495
页数:11
相关论文
共 100 条
[11]   Are immunological mechanisms involved in colon cancer and are they possible markers for biotherapy improvement? [J].
Berghella, Anna Maria ;
Contasta, Ida ;
Pellegrini, Patrizia ;
Del Beato, Tiziana ;
Adorno, Domenico .
CANCER BIOTHERAPY AND RADIOPHARMACEUTICALS, 2006, 21 (05) :468-487
[12]   Ageing gender-specific "Biomarkers of Homeostasis", to protect ourselves against the diseases of the old age [J].
Berghella, Anna Maria ;
Contasta, Ida ;
Marulli, Giuseppe ;
D'Innocenzo, Carlo ;
Garofalo, Ferdinando ;
Gizzi, Francesca ;
Bartolomucci, Marco ;
Laglia, Giacomo ;
Valeri, Marisa ;
Gizzi, Mario ;
Friscioni, Mauro ;
Barone, Mario ;
Del Beato, Tiziana ;
Secinaro, Enzo ;
Pellegrini, Patrizia .
IMMUNITY & AGEING, 2014, 11
[13]   The discovery of how gender influences age immunological mechanisms in health and disease, and the identification of ageing gender-specific biomarkers, could lead to specifically tailored treatment and ultimately improve therapeutic success rates [J].
Berghella, Anna Maria ;
Contasta, Ida ;
Del Beato, Tiziana ;
Pellegrini, Patrizia .
IMMUNITY & AGEING, 2012, 9
[14]   Reciprocal developmental pathways for the generation of pathogenic effector TH17 and regulatory T cells [J].
Bettelli, E ;
Carrier, YJ ;
Gao, WD ;
Korn, T ;
Strom, TB ;
Oukka, M ;
Weiner, HL ;
Kuchroo, VK .
NATURE, 2006, 441 (7090) :235-238
[15]  
BRADLEY LM, 1995, J IMMUNOL, V155, P1713
[16]   INFLUENCE OF SEX ON IMMUNOGLOBULIN LEVELS [J].
BUTTERWO.M ;
MCCLELLA.B ;
ALLANSMI.M .
NATURE, 1967, 214 (5094) :1224-&
[17]   Immunogenetics, gender, and longevity [J].
Candore, Giuseppina ;
Balistreri, Carmela R. ;
Listi, Florinda ;
Grimaldi, Maria P. ;
Vasto, Sonya ;
Colonna-Romano, Giuseppina ;
Franceschi, Claudio ;
Lio, Domenico ;
Caselli, Graziella ;
Caruso, Calogero .
ESTROGENS AND HUMAN DISEASES, 2006, 1089 :516-537
[18]   Gender differences in host defense mechanisms [J].
Cannon, JG ;
Pierre, BAS .
JOURNAL OF PSYCHIATRIC RESEARCH, 1997, 31 (01) :99-113
[19]   Personalized Colon Cancer Care in 2010 [J].
Catenacci, Daniel V. T. ;
Kozloff, Mark ;
Kindler, Hedy L. ;
Polite, Blase .
SEMINARS IN ONCOLOGY, 2011, 38 (02) :284-308
[20]   TGF-β1:: immunosuppressant and viability factor for T lymphocytes [J].
Cerwenka, A ;
Swain, SL .
MICROBES AND INFECTION, 1999, 1 (15) :1291-1296