| Literature DB >> 26590477 |
Keith I Block1, Charlotte Gyllenhaal2, Leroy Lowe3, Amedeo Amedei4, A R M Ruhul Amin5, Amr Amin6, Katia Aquilano7, Jack Arbiser8, Alexandra Arreola9, Alla Arzumanyan10, S Salman Ashraf11, Asfar S Azmi12, Fabian Benencia13, Dipita Bhakta14, Alan Bilsland15, Anupam Bishayee16, Stacy W Blain17, Penny B Block2, Chandra S Boosani18, Thomas E Carey19, Amancio Carnero20, Marianeve Carotenuto21, Stephanie C Casey22, Mrinmay Chakrabarti23, Rupesh Chaturvedi24, Georgia Zhuo Chen5, Helen Chen25, Sophie Chen26, Yi Charlie Chen27, Beom K Choi28, Maria Rosa Ciriolo7, Helen M Coley29, Andrew R Collins30, Marisa Connell25, Sarah Crawford31, Colleen S Curran32, Charlotta Dabrosin33, Giovanna Damia34, Santanu Dasgupta35, Ralph J DeBerardinis36, William K Decker37, Punita Dhawan38, Anna Mae E Diehl39, Jin-Tang Dong5, Q Ping Dou12, Janice E Drew40, Eyad Elkord41, Bassel El-Rayes42, Mark A Feitelson10, Dean W Felsher22, Lynnette R Ferguson43, Carmela Fimognari44, Gary L Firestone45, Christian Frezza46, Hiromasa Fujii47, Mark M Fuster48, Daniele Generali49, Alexandros G Georgakilas50, Frank Gieseler51, Michael Gilbertson52, Michelle F Green53, Brendan Grue54, Gunjan Guha14, Dorota Halicka55, William G Helferich56, Petr Heneberg57, Patricia Hentosh58, Matthew D Hirschey59, Lorne J Hofseth60, Randall F Holcombe61, Kanya Honoki47, Hsue-Yin Hsu62, Gloria S Huang63, Lasse D Jensen64, Wen G Jiang65, Lee W Jones66, Phillip A Karpowicz67, W Nicol Keith15, Sid P Kerkar68, Gazala N Khan69, Mahin Khatami70, Young H Ko71, Omer Kucuk5, Rob J Kulathinal10, Nagi B Kumar72, Byoung S Kwon73, Anne Le74, Michael A Lea75, Ho-Young Lee76, Terry Lichtor77, Liang-Tzung Lin78, Jason W Locasale79, Bal L Lokeshwar80, Valter D Longo81, Costas A Lyssiotis82, Karen L MacKenzie83, Meenakshi Malhotra84, Maria Marino85, Maria L Martinez-Chantar86, Ander Matheu87, Christopher Maxwell25, Eoin McDonnell53, Alan K Meeker88, Mahya Mehrmohamadi89, Kapil Mehta90, Gregory A Michelotti39, Ramzi M Mohammad12, Sulma I Mohammed91, D James Morre92, Vinayak Muralidhar93, Irfana Muqbil12, Michael P Murphy94, Ganji Purnachandra Nagaraju42, Rita Nahta5, Elena Niccolai95, Somaira Nowsheen96, Carolina Panis97, Francesco Pantano98, Virginia R Parslow43, Graham Pawelec99, Peter L Pedersen100, Brad Poore74, Deepak Poudyal60, Satya Prakash84, Mark Prince101, Lizzia Raffaghello102, Jeffrey C Rathmell53, W Kimryn Rathmell9, Swapan K Ray23, Jörg Reichrath103, Sarallah Rezazadeh104, Domenico Ribatti105, Luigi Ricciardiello106, R Brooks Robey107, Francis Rodier108, H P Vasantha Rupasinghe109, Gian Luigi Russo110, Elizabeth P Ryan111, Abbas K Samadi112, Isidro Sanchez-Garcia113, Andrew J Sanders65, Daniele Santini98, Malancha Sarkar114, Tetsuro Sasada115, Neeraj K Saxena116, Rodney E Shackelford117, H M C Shantha Kumara118, Dipali Sharma119, Dong M Shin5, David Sidransky120, Markus David Siegelin121, Emanuela Signori122, Neetu Singh123, Sharanya Sivanand124, Daniel Sliva125, Carl Smythe126, Carmela Spagnuolo110, Diana M Stafforini127, John Stagg128, Pochi R Subbarayan129, Tabetha Sundin130, Wamidh H Talib131, Sarah K Thompson132, Phuoc T Tran133, Hendrik Ungefroren51, Matthew G Vander Heiden134, Vasundara Venkateswaran135, Dass S Vinay136, Panagiotis J Vlachostergios137, Zongwei Wang138, Kathryn E Wellen124, Richard L Whelan118, Eddy S Yang139, Huanjie Yang140, Xujuan Yang56, Paul Yaswen141, Clement Yedjou142, Xin Yin48, Jiyue Zhu143, Massimo Zollo21.
Abstract
Targeted therapies and the consequent adoption of "personalized" oncology have achieved notable successes in some cancers; however, significant problems remain with this approach. Many targeted therapies are highly toxic, costs are extremely high, and most patients experience relapse after a few disease-free months. Relapses arise from genetic heterogeneity in tumors, which harbor therapy-resistant immortalized cells that have adopted alternate and compensatory pathways (i.e., pathways that are not reliant upon the same mechanisms as those which have been targeted). To address these limitations, an international task force of 180 scientists was assembled to explore the concept of a low-toxicity "broad-spectrum" therapeutic approach that could simultaneously target many key pathways and mechanisms. Using cancer hallmark phenotypes and the tumor microenvironment to account for the various aspects of relevant cancer biology, interdisciplinary teams reviewed each hallmark area and nominated a wide range of high-priority targets (74 in total) that could be modified to improve patient outcomes. For these targets, corresponding low-toxicity therapeutic approaches were then suggested, many of which were phytochemicals. Proposed actions on each target and all of the approaches were further reviewed for known effects on other hallmark areas and the tumor microenvironment. Potential contrary or procarcinogenic effects were found for 3.9% of the relationships between targets and hallmarks, and mixed evidence of complementary and contrary relationships was found for 7.1%. Approximately 67% of the relationships revealed potentially complementary effects, and the remainder had no known relationship. Among the approaches, 1.1% had contrary, 2.8% had mixed and 62.1% had complementary relationships. These results suggest that a broad-spectrum approach should be feasible from a safety standpoint. This novel approach has potential to be relatively inexpensive, it should help us address stages and types of cancer that lack conventional treatment, and it may reduce relapse risks. A proposed agenda for future research is offered.Entities:
Keywords: Cancer hallmarks; Integrative medicine; Multi-targeted; Phytochemicals; Targeted therapy
Mesh:
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Year: 2015 PMID: 26590477 PMCID: PMC4819002 DOI: 10.1016/j.semcancer.2015.09.007
Source DB: PubMed Journal: Semin Cancer Biol ISSN: 1044-579X Impact factor: 15.707