Pleiotropic Effects of Modified Citrus Pectin

被引:88
作者
Eliaz, Isaac [1 ]
Raz, Avraham [2 ,3 ,4 ]
机构
[1] Amitabha Med Clin & Healing Ctr, 398 Tesconi Ct, Santa Rosa, CA 95401 USA
[2] Wayne State Univ, Sch Med, Dept Oncol, 4100 John R St, Detroit, MI 48201 USA
[3] Wayne State Univ, Sch Med, Dept Pathol, 4100 John R St, Detroit, MI 48201 USA
[4] Barbara Ann Karmanos Canc Inst, 4100 John R St, Detroit, MI 48201 USA
关键词
cancer; cardiovascular; fibrosis; galectin; inflammation; pectasol; PROSTATE-CANCER CELLS; HUMAN BREAST; GALECTIN-3; INHIBITION; PHARMACOLOGICAL INHIBITION; INDUCED APOPTOSIS; CYCLE ARREST; GROWTH; EXPRESSION; ADHESION; CARCINOMA;
D O I
10.3390/nu11112619
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Modified citrus pectin (MCP) has a low-molecular-weight degree of esterification to allow absorption from the small intestinal epithelium into the circulation. MCP produces pleiotropic effects, including but not limited to its antagonism of galectin-3, which have shown benefit in preclinical and clinical models. Regarding cancer, MCP modulates several rate-limiting steps of the metastatic cascade. MCP can also affect cancer cell resistance to chemotherapy. Regarding fibrotic diseases, MCP modulates many of the steps involved in the pathogenesis of aortic stenosis. MCP also reduces fibrosis to the kidney, liver, and adipose tissue. Other benefits of MCP include detoxification and improved immune function. This review summarizes the pleiotropic effects of MCP.
引用
收藏
页数:18
相关论文
共 124 条
[1]   Modified citrus pectin stops progression of liver fibrosis by inhibiting galectin-3 and inducing apoptosis of stellate cells [J].
Abu-Elsaad, Nashwa M. ;
Elkashef, Wagdi Fawzi .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 2016, 94 (05) :554-562
[2]  
Akahani S, 1997, CANCER RES, V57, P5272
[3]   Intravascular origin of metastasis from the proliferation of endothelium-attached tumor cells: a new model for metastasis [J].
Al-Mehdi, AB ;
Tozawa, K ;
Fisher, AB ;
Shientag, L ;
Lee, A ;
Muschel, RJ .
NATURE MEDICINE, 2000, 6 (01) :100-102
[4]  
Arrieta V, 2019, AN SIST SANIT NAVAR, V42, P199, DOI [10.23938/assn.0643, 10.23938/ASSN.0643]
[5]   A role for galectin-3 in the development of early molecular alterations in short-term aortic stenosis [J].
Arrieta, Vanessa ;
Martinez-Martinez, Ernesto ;
Ibarrola, Jaime ;
Alvarez, Virginia ;
Sadaba, Rafael ;
Garcia-Pena, Amaia ;
Fernandez-Celis, Amaya ;
Cachofeiro, Victoria ;
Rossignol, Patrick ;
Lopez-Andres, Natalia .
CLINICAL SCIENCE, 2017, 131 (10) :935-949
[6]  
Azemar M, 2007, CLIN MED INSIGHTS-ON, V1, P73
[7]   Galectin-3 Activates PPARγ and Supports White Adipose Tissue Formation and High-Fat Diet-Induced Obesity [J].
Baek, Jung-Hwan ;
Kim, Seok-Jun ;
Kang, Hyeok Gu ;
Lee, Hyun-Woo ;
Kim, Jung-Hoon ;
Hwang, Kyung-A ;
Song, Jaewhan ;
Chun, Kyung-Hee .
ENDOCRINOLOGY, 2015, 156 (01) :147-156
[8]   The Impact of Galectin-3 Inhibition on Aldosterone-Induced Cardiac and Renal Injuries [J].
Calvier, Laurent ;
Martinez-Martinez, Ernesto ;
Miana, Maria ;
Cachofeiro, Victoria ;
Rousseau, Elodie ;
Rafael Sadaba, J. ;
Zannad, Faiez ;
Rossignol, Patrick ;
Lopez-Andres, Natalia .
JACC-HEART FAILURE, 2015, 3 (01) :59-67
[9]   Galectin-3 Mediates Aldosterone-Induced Vascular Fibrosis [J].
Calvier, Laurent ;
Miana, Maria ;
Reboul, Pascal ;
Cachofeiro, Victoria ;
Martinez-Martinez, Ernesto ;
de Boer, Rudolf A. ;
Poirier, Francoise ;
Lacolley, Patrick ;
Zannad, Faiez ;
Rossignol, Patrick ;
Lopez-Andres, Natalia .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2013, 33 (01) :67-+
[10]   Dissemination and growth of cancer cells in metastatic sites [J].
Chambers, AF ;
Groom, AC ;
MacDonald, IC .
NATURE REVIEWS CANCER, 2002, 2 (08) :563-572