Curcumin for monoclonal gammopathies. What can we hope for, what should we fear?

被引:4
|
作者
Vermorken, A. J. M. [1 ]
Zhu, J. [1 ]
Van de Ven, W. J. M. [1 ]
Andres, E. [2 ]
机构
[1] Katholieke Univ Leuven, Dept Human Genet, Mol Oncol Lab, BE-3000 Louvain, Belgium
[2] Univ Hosp Strasbourg, Dept Internal Med Diabet & Metab Disorders, Strasbourg, France
关键词
Monoclonal gammopathy; Multiple myeloma; Clinical trials; Immunosuppression; Dendritic cells; Curcumin; Inflammation; Clonogenic growth; HUMAN MULTIPLE-MYELOMA; REGULATORY T-CELLS; UNDETERMINED SIGNIFICANCE MGUS; DENDRITIC CELLS; BONE-MARROW; ACTIVATING FACTOR; B-LYMPHOCYTE; PLASMA-CELLS; IN-VITRO; PROGRESSION;
D O I
10.1016/j.critrevonc.2012.04.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Over the last decades there has been an increasing interest in a possible role of curcumin on cancer. Although curcumin is considered safe for healthy people, conclusive evidence on the safety and efficacy of curcumin for patients with monoclonal gammopathies is, so far, lacking. The present paper reviews the literature on molecular, cellular and clinical effects of curcumin in an attempt to identify, reasons for optimism but also for concern. The results of this critical evaluation can be useful for both patient- selection and monitoring in the context of clinical trials. Curcumin might be helpful for some but certainly not for all patients with monoclonal gammopathies. It is important to avoid unnecessary detrimental side effects in some in order to safeguard curcumin for those that could benefit. Parameters for patient monitoring, that can be used as early warning signs and as indicators of a favorable development have therefore been suggested. (c) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:350 / 360
页数:11
相关论文
共 50 条
  • [1] Monoclonal gammopathy of undetermined significance and biological treatments: What should we do?
    Lemieux-Blanchard, Emilie
    JOINT BONE SPINE, 2017, 84 (06) : 651 - 653
  • [2] Concise Review: Human Embryonic Stem Cells-What Have We Done? What Are We Doing? Where Are We Going?
    Ilic, Dusko
    Ogilvie, Caroline
    STEM CELLS, 2017, 35 (01) : 17 - 25
  • [3] Immune privilege of skin stem cells: What do we know and what can we learn?
    Agudo, Judith
    EXPERIMENTAL DERMATOLOGY, 2021, 30 (04) : 522 - 528
  • [4] Biocompatibility of new peritoneal dialysis solutions:: What can we hope to achieve?
    Chung, SH
    Stenvinkel, P
    Bergström, J
    Lindholm, B
    PERITONEAL DIALYSIS INTERNATIONAL, 2000, 20 : S57 - S67
  • [5] Immunity to Avian Leukosis Virus: Where Are We Now and What Should We Do?
    Feng, Min
    Zhang, Xiquan
    FRONTIERS IN IMMUNOLOGY, 2016, 7
  • [6] What should we expect from psychotherapy?
    Goldfried, Marvin R.
    CLINICAL PSYCHOLOGY REVIEW, 2013, 33 (07) : 862 - 869
  • [7] Dendritic cell-based therapeutic cancer vaccines: what we have and what we need
    Kalinski, Pawel
    Urban, Julie
    Narang, Rahul
    Berk, Erik
    Wieckowski, Ewa
    Muthuswamy, Ravikumar
    FUTURE ONCOLOGY, 2009, 5 (03) : 379 - 390
  • [8] Paradoxical side effects of bisphosphonates on the skeleton: What do we know and what can we do?
    Vargas-Franco, Jorge W.
    Castaneda, Beatriz
    Redini, Francoise
    Gomez, David F.
    Heymann, Dominique
    Lezot, Frederic
    JOURNAL OF CELLULAR PHYSIOLOGY, 2018, 233 (08) : 5696 - 5715
  • [9] Memory T cell subsets in tuberculosis: What should we be targeting?
    Henao-Tamayo, Marcela
    Ordway, Diane J.
    Orme, Ian M.
    TUBERCULOSIS, 2014, 94 (05) : 455 - 461
  • [10] Managing recurrent otitis externa in dogs: what have we learned and what can we do better?
    Nuttall, Tim
    JAVMA-JOURNAL OF THE AMERICAN VETERINARY MEDICAL ASSOCIATION, 2023, 261 : S10 - S22