Designing a broad-spectrum integrative approach for cancer prevention and treatment

  • Keith I. Block
  • , Charlotte Gyllenhaal
  • , Leroy Lowe
  • , Amedeo Amedei
  • , A. R.M. Ruhul Amin
  • , Amr Amin
  • , Katia Aquilano
  • , Jack Arbiser
  • , Alexandra Arreola
  • , Alla Arzumanyan
  • , S. Salman Ashraf
  • , Asfar S. Azmi
  • , Fabian Benencia
  • , Dipita Bhakta
  • , Alan Bilsland
  • , Anupam Bishayee
  • , Stacy W. Blain
  • , Penny B. Block
  • , Chandra S. Boosani
  • , Thomas E. Carey
  • Amancio Carnero, Marianeve Carotenuto, Stephanie C. Casey, Mrinmay Chakrabarti, Rupesh Chaturvedi, Georgia Zhuo Chen, Helen Chen, Sophie Chen, Yi Charlie Chen, Beom K. Choi, Maria Rosa Ciriolo, Helen M. Coley, Andrew R. Collins, Marisa Connell, Sarah Crawford, Colleen S. Curran, Charlotta Dabrosin, Giovanna Damia, Santanu Dasgupta, Ralph J. DeBerardinis, William K. Decker, Punita Dhawan, Anna Mae E. Diehl, Jin Tang Dong, Q. Ping Dou, Janice E. Drewa, Eyad Elkord, Bassel El-Rayes, Mark A. Feitelson, Dean W. Felsheru, Lynnette R. Ferguson, Carmela Fimognari, Gary L. Firestone, Christian Frezza, Hiromasa Fujii, Mark M. Fuster, Daniele Generali, Alexandros G. Georgakilas, Frank Gieseler, Michael Gilbertson, Michelle F. Green, Brendan Grue, Gunjan Guhal, Dorota Halicka, William G. Helferich, Petr Heneberg, Patricia Hentosh, Matthew D. Hirschey, Lorne J. Hofseth, Randall F. Holcombe, Kanya Honoki, Hsue Yin Hsu, Gloria S. Huang, Lasse D. Jensen, Wen G. Jiang, Lee W. Jones, Phillip A. Karpowicz, W. Nicol Keith, Sid P. Kerkar, Gazala N. Khan, Mahin Khatami, Young H. Ko, Omer Kucuk, Rob J. Kulathinal, Nagi B. Kumar, Byoung S. Kwon, Anne Leb, Michael A. Leab, Ho Young Lee, Terry Lichtor, Liang Tzung Lin, Jason W. Locasale, Bal L. Lokeshwar, Valter D. Longo, Costas A. Lyssiotis, Karen L. MacKenzie, Meenakshi Malhotra, Maria Marino, Maria L. Martinez-Chantar, Ander Matheu, Christopher Maxwellx, Eoin McDonnell, Alan K. Meeker, Mahya Mehrmohamadi, Kapil Mehta, Gregory A. Michelotti, Ramzi M. Mohammad, Sulma I. Mohammed, D. James Morre, Irfana Muqbil, Vinayak Muralidharcq, Michael P. Murphy, Ganji Purnachandra Nagaraju, Rita Nahta, Elena Niccolai, Somaira Nowsheen, Carolina Panis, Francesco Pantano, Virginia R. Parslow, Graham Pawelec, Peter L. Pedersen, Brad Poore, Deepak Poudyal, Satya Prakash, Mark Prince, Lizzia Raffaghello, Jeffrey C. Rathmell, W. Kimryn Rathmell, Swapan K. Ray, Jörg Reichrath, Sarallah Rezazadeh, Domenico Ribatti, Luigi Ricciardiello, R. Brooks Robeydf, Francis Rodierdh, H. P.Vasantha Rupasinghe, Gian Luigi Russo, Elizabeth P. Ryan, Abbas K. Samadi, Isidro Sanchez-Garcia, Andrew J. Sanders, Daniele Santini, Malancha Sarkar, Tetsuro Sasada, Neeraj K. Saxena, Rodney E. Shackelford, H. M.C. Shantha Kumara, Dipali Sharma, Dong M. Shin, David Sidransky, Markus David Siegelin, Emanuela Signori, Neetu Singh, Sharanya Sivanand, Daniel Sliva, Carl Smythe, Carmela Spagnuolo, Diana M. Stafforini, John Stagg, Pochi R. Subbarayan, Tabetha Sundin, Wamidh H. Talib, Sarah K. Thompson, Phuoc T. Tran, Hendrik Ungefroren, Matthew G. Vander Heiden, Vasundara Venkateswaran, Dass S. Vinay, Panagiotis J. Vlachostergios, Zongwei Wang, Kathryn E. Wellen, Richard L. Whelan, Eddy S. Yang, Huanjie Yang, Xujuan Yang, Paul Yaswen, Clement Yedjou, Xin Yin, Jiyue Zhu, Massimo Zollo

Research output: Contribution to journalReview articlepeer-review

295 Scopus citations

Abstract

Targeted therapies and the consequent adoption of "personalized" oncology have achieved notablesuccesses in some cancers; however, significant problems remain with this approach. Many targetedtherapies are highly toxic, costs are extremely high, and most patients experience relapse after a fewdisease-free months. Relapses arise from genetic heterogeneity in tumors, which harbor therapy-resistantimmortalized cells that have adopted alternate and compensatory pathways (i.e., pathways that are notreliant upon the same mechanisms as those which have been targeted). To address these limitations, aninternational 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 aspectsof relevant cancer biology, interdisciplinary teams reviewed each hallmark area and nominated a widerange of high-priority targets (74 in total) that could be modified to improve patient outcomes. For thesetargets, corresponding low-toxicity therapeutic approaches were then suggested, many of which werephytochemicals. Proposed actions on each target and all of the approaches were further reviewed forknown effects on other hallmark areas and the tumor microenvironment. Potential contrary or procar-cinogenic effects were found for 3.9% of the relationships between targets and hallmarks, and mixedevidence of complementary and contrary relationships was found for 7.1%. Approximately 67% of therelationships 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. Thisnovel approach has potential to be relatively inexpensive, it should help us address stages and types ofcancer that lack conventional treatment, and it may reduce relapse risks. A proposed agenda for futureresearch is offered.

Original languageEnglish
Pages (from-to)S276-S304
JournalSeminars in Cancer Biology
Volume35
DOIs
StatePublished - 2015

Bibliographical note

Publisher Copyright:
© 2015 The Authors.

Funding

FundersFunder number
National Institutes of Health (NIH)
European Commission
UK Medical Research Council, Engineering and Physical Sciences Research CouncilMC_UU_12022/6, MC_UP_1101/3, MC_U105663142
National Childhood Cancer Registry – National Cancer InstituteF32CA177139, R21CA155686, R01CA170378, R01CA131294, U54CA149145, R01CA156776, F31CA154080, R21CA169757, R15CA137499, R21CA185943, R01CA151304, R00CA168997, R01CA164095, R21CA188818, R01CA100816, U54CA143907, R01CA010951, R01CA120009, R01CA166348, R01CA127258, R01CA109335, R33CA161873, R01CA028704, P01CA073992, T32CA059365, P30CA008748, R21CA184788, R03CA171326, P30CA022453
National Institute of Diabetes and Digestive and Kidney DiseasesK01DK077137, R03DK089130
National Institute of General Medical Sciences DP2GM119177 Sophie Dumont National Institute of General Medical SciencesR01GM071725, P20GM103434
National Institute of Arthritis and Musculoskeletal and Skin DiseasesR01AR047901
National Center for Research ResourcesP20RR016477
Institute of Neurological Disorders and Stroke National Advisory Neurological Disorders and Stroke CouncilK08NS083732
Japan Society for the Promotion of Science15K10455
Seventh Framework Programme303514, 201662, 311876, 259679, 278570, 282891
U.S. Department of Veterans AffairsI01BX001517
National Institute of Allergy and Infectious F32-AI286447 Cydney N. Johnson Diseases National Institute of Allergy and Infectious R01AI168214 Jason W. Rosch Diseases National Institute of Allergy and Infectious P30 Cydney N. Johnson Diseases National Institute of Allergy and Infectious R00-AI166116 Christopher D. Radka Diseases National Institute of Allergy and Infectious T32-AI106700 Cydney N. Johnson Diseases National Institute of Allergy and Infectious R01AI192221 Jason W. Rosch Diseases National Inst...R01AI110613, R01AI076535
National Heart, Lung, and Blood Institute (NHLBI)T32HL098062, R01HL107652, R01HL108006
National Institute on Minority Health and Health Disparities (NIMHD)G12MD007581
National Institutes of Health/National Institute of Environmental Health SciencesU01ES019458
National Institute on AgingP30AG028716, R01AG045351, R01AG020642, P01AG034906
National Center for Complementary and Integrative HealthK01AT007324, P01AT003961

    Keywords

    • Cancer hallmarks
    • Integrative medicine
    • Multi-targeted
    • Phytochemicals
    • Targeted therapy

    ASJC Scopus subject areas

    • Cancer Research

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