Genistein

"目录号: HY-14596

Protein Tyrosine Kinase/RTKJAK/STAT SignalingAutophagy-

Genistein 是一种有效的蛋白酪氨酸激酶 (PTK) 抑制剂,抑制EGFRIC50为 0.7 μg/mL (0.6 μM)。

EGFRAutophagy

相关产品

Cycloheximide-TAK-242-LY294002-3-Methyladenine-(+)-JQ-1-SB 203580-SP600125-U0126-Enzalutamide-Actinomycin D-Olaparib-Doxorubicin hydrochloride-AZD-9291-Dorsomorphin dihydrochloride-Mitomycin C-

生物活性

Description

Genistein is a potent inhibitor of the protein tyrosine kinase (PTK) activity of theEGFRin vitro with anIC50of 0.7 μg/mL (0.6 μM).

IC50& Target

IC50: 0.7 μg/mL (0.6 μM) (EGFR)[1]

In Vitro

Genistein inhibits serum-stimulated growth of MCF-7 and T47D ER+cells with IC50values of 7.6 and 8.7 μg/mL by dye exclusion, respectively, and 8.7 and 10.6 μg/mL by [3H]thymidmne incorporation, respectively. These values are similar to the IC50values of 9.4 and 7 μg/mL for MCF-7 and T47D ER+cells, respectively, obtained with the MTT assay. Additionally, Genistein at concentrations up to 20 μg/mL does not alter MTT mitochondrial reduction when compared to control cells in an 8 h incubation period. Furthermore, neither biochanin A or daidzein are found to interfere with the MTT assay at IC50concentrations. Therefore, the MTT assay is valid for determining growth inhibition by Genistein at concentrations under 20 μg/mL in the systems studied[1].

In Vivo

In the present study, the effective dose of morphine caused a significant decrease in testis weight of mice compared to Saline group (p=0.00). Moreover, testis weight are significantly increase in treated animals with Genistein and Genistein plus morphine in all doses in comparison with morphine group (p=0.028). Morphine caused a significant decrease in the testosterone, LH and FSH hormones compared to saline group (p=0.00). In addition, the testosterone, LH and FSH hormones increased significantly in Genistein (p<0.05) and Genistein plus morphine in all groups administration compared to morphine group (p=0.024)[2]. Bisphenol A (BPA) treatment alone and combined with Genistein had no significant effect on the protein expression of LC3II and PPARα in liver of STD- or HFD-fed rats (P>0.05; P>0.05). Significant decreasing of the protein expression of PPARγ in liver is observed when Genistein is added to rats, compared to either HFD group or HFD-BPA group[3].

Clinical Trial

NCT01985763

Sofya Pintova-DSM Nutritional Products, Inc.-Icahn School of Medicine at Mount Sinai

Colon Cancer-Rectal Cancer-Colorectal Cancer

November 2013

Phase 1-Phase 2

NCT02499861

St. Justine's Hospital

Cancer

July 2015

Phase 1-Phase 2

NCT00882765

Jonsson Comprehensive Cancer Center-National Cancer Institute (NCI)

Pancreatic Cancer

May 2009

Phase 2

NCT02796794

TC Erciyes University

Sepsis

June 2015

Phase 4

NCT00769990

Masonic Cancer Center, University of Minnesota

Breast Cancer-Kidney Cancer-Lung Cancer-Melanoma-Metastatic Cancer-Pain-Prostate Cancer

September 2008

Phase 1-Phase 2

NCT01982578

Fundación para la Investigación del Hospital Clínico de Valencia-University of Valencia

Alzheimer's Disease

November 2013

NCT01126879

Northwestern University-National Cancer Institute (NCI)

Adenocarcinoma of the Prostate-Recurrent Prostate Cancer-Stage I Prostate Cancer-Stage II Prostate Cancer-Stage III Prostate Cancer

May 2010

Phase 2

NCT00541710

University of Messina-Ministry of Education, Universities and Research, Italy

Metabolic Syndrome

October 2007

Phase 2-Phase 3

NCT02766478

Emory University

Prostate Cancer

August 1, 2017

Phase 2

NCT01489813

Emory University

Bladder Cancer

May 19, 2017

Phase 2

NCT02624388

University of Virginia

Lymphoma-Childhood Lymphoma-Solid Tumor-Childhood Solid Tumor-Neuroblastoma-Ewing Sarcoma-Hodgkin Lymphoma-Non-Hodgkin Lymphoma-Rhabdomyosarcoma-Soft Tissue Sarcoma-Medulloblastoma-Germ Cell Tumor-Wilms Tumor-Brain Neoplasms-Medulloblastoma, Childhood-Neuroectodermal Tumors, Primitive

August 2016

Phase 2

NCT01325311

National Cancer Institute (NCI)

Prostate Adenocarcinoma-Stage I Prostate Cancer-Stage IIA Prostate Cancer-Stage IIB Prostate Cancer

December 2011

Phase 2

NCT00626769

University of Messina-Primus Pharmaceuticals

Menopause-Osteopenia

July 2005

Phase 2-Phase 3

NCT00276835

Northwestern University-National Cancer Institute (NCI)

Kidney Cancer-Melanoma (Skin)

November 2005

Early Phase 1

NCT00590538

Children's Hospital of Philadelphia-Cystic Fibrosis Foundation Therapeutics

Cystic Fibrosis

February 2003

Phase 1-Phase 2

NCT01628471

Uman Pharma-DSM Nutritional Products, Inc.-MDEIE Ministry, Québec Government-INRS-Institut Armand Frappier , Université du Québec

Non Small Cell Lung Cancer

November 2012

Phase 1-Phase 2

NCT00016744

Children's Hospital of Philadelphia-Cystic Fibrosis Foundation Therapeutics-National Center for Research Resources (NCRR)

Cystic Fibrosis

September 2001

Phase 1-Phase 2

NCT01664650

University of Messina-Ministry of Education, Universities and Research, Italy

Metabolic Syndrome

September 2008

Phase 2-Phase 3

NCT03040531

University of Messina-Ministry of Health, Italy

Osteoporosis, Steroid Induced

January 19, 2017

Phase 2-Phase 3

NCT00244933

Barbara Ann Karmanos Cancer Institute-National Cancer Institute (NCI)

Breast Cancer

February 2004

Phase 2

NCT01538316

University of Hohenheim-University Hospital Tuebingen-Quercegen Pharmaceuticals

Primary Prevention of Prostate Cancer

March 2012

NCT00099008

UNC Lineberger Comprehensive Cancer Center-National Cancer Institute (NCI)

Breast Cancer-Endometrial Cancer

March 2004

Phase 1

NCT00058266

Northwestern University-National Cancer Institute (NCI)

Prostate Cancer

December 2002

Phase 2

NCT00001696

National Cancer Institute (NCI)-National Institutes of Health Clinical Center (CC)

Cancer

April 1998

Phase 1

NCT00118040

National Cancer Institute (NCI)

Recurrent Bladder Cancer-Stage I Bladder Cancer-Stage II Bladder Cancer-Stage III Bladder Cancer

June 2005

Phase 2

NCT00005827

UNC Lineberger Comprehensive Cancer Center-National Cancer Institute (NCI)

Prostate Cancer

December 1999

Phase 1

NCT00546039

University Hospital, Aker

Prostatic Neoplasms

April 2007

Phase 2

NCT00290758

National Cancer Institute (NCI)

Breast Cancer

January 2006

Phase 2

NCT00584532

University of California, Davis

Prostate Cancer

November 2003

Phase 2-Phase 3

NCT00287690

Imperial College London

Coronary Artery Disease

October 1999

Phase 2-Phase 3

NCT00355953

University of Messina

Menopause-Osteopenia

January 2003

Phase 2-Phase 3

NCT00269555

University of California, Davis

Prostate Cancer

May 2004

NCT00951912

Sun Yat-sen University-Chinese Nutrition Society-Danone Institute International-Department of Health of Guangdong Province

Type 2 Diabetes Mellitus

August 2009

NCT00376948

Barbara Ann Karmanos Cancer Institute-National Cancer Institute (NCI)

Pancreatic Cancer

May 2005

Phase 2

NCT00244907

Purdue University-National Center for Complementary and Integrative Health (NCCIH)-Office of Dietary Supplements (ODS)

Osteoporosis-Osteopenia

January 2006

Phase 1

NCT00004858

Parker Hughes Cancer Center-National Cancer Institute (NCI)

Leukemia-Lymphoma

March 2000

Phase 1

NCT00000613

National Heart, Lung, and Blood Institute (NHLBI)

Bone Diseases-Cardiovascular Diseases-Coronary Disease-Depression-Heart Diseases-Myocardial Ischemia-Osteoporosis-Postmenopause

April 1997

Phase 2

NCT01556737

Wageningen University

Postmenopause

November 2011

NCT00499408

Wake Forest University Health Sciences-National Cancer Institute (NCI)

Prostate Cancer

April 2007

Phase 2

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References

[1].Peterson G, et al. Genistein inhibits both estrogen and growth factor-stimulated proliferation of human breast cancer cells. Cell Growth Differ. 1996 Oct;7(10):1345-51.

[2].Jalili C, et al. Effect of Genistein on reproductive parameter and serum nitric oxide levels in morphine-treated mice. Int J Reprod Biomed (Yazd). 2016 Feb;14(2):95-102.

[3].Ding S, et al. Environmentally Relevant Dose of Bisphenol A Does Not Affect Lipid Metabolism and Has No Synergetic or Antagonistic Effects on Genistein's Beneficial Roles on Lipid Metabolism. PLoS One. 2016 May 12;11(5):e0155352.

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