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  1. General Info
  2. Source Info
  3. Effects Info
  4. Reference
Phytochemical Details
01. General Information
Name Resveratrol
PubChem CID 445154
Molecular Weight 228.24g/mol
Synonyms

3,4',5-stilbenetriol, 3,4',5-Trihydroxystilbene, 3,5,4'-trihydroxystilbene, cis Resveratrol, cis-resveratrol, resveratrol, Resveratrol 3 sulfate, Resveratrol, (Z)-, resveratrol-3-sulfate, SRT 501, SRT-501, SRT501, trans Resveratrol, trans Resveratrol 3 O sulfate, trans-resveratrol, trans-resveratrol-3-O-sulfate

Formula C₁₄H₁₂O₃
SMILES C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O
InChI 1S/C14H12O3/c15-12-5-3-10(4-6-12)1-2-11-7-13(16)9-14(17)8-11/h1-9,15-17H/b2-1+
InChIKey LUKBXSAWLPMMSZ-OWOJBTEDSA-N
CAS Number 501-36-0
ChEMBL ID CHEMBL165
ChEBI ID CHEBI:27881
Herb ID HBIN042111
Drug Bank ID DB02709
KEGG ID C03582
Toxicity Organism Test Type Route(Dose)
rat LD50 intraperitoneal(165 mg/kg)
mouse LD50 intraperitoneal(254 mg/kg)
rat LD50 oral(322 mg/kg)
Structure 2D-img
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2D MOL 3D MOL
02. Source Information of Phytochemical
(1) Stemona sessilifolia Warm
Chineses Pinyin BaiBu
Use Part Root
Habitat HuBei, GuangDong, FuJian, SiChuan, GuiZhou
Flavor Sweet, Bitter
Meridian Tropism Lung
Species
>Kingdom: Viridiplantae
 -->Phylum: Streptophyta
  -->Class: Equisetopsida
   -->Order: Pandanales
    -->Family: Stemonaceae
     -->Genus: Stemona
      -->Species: Stemona sessilifolia
(2) Gnetum parvifolium Warm
Chineses Pinyin XiaoYeMaiMaTeng
Use Part Root; leaf; Rattan
Habitat FuJian, GuangXi, GuangDong, YunNan
Flavor Bitter
Species
>Kingdom: Viridiplantae
 -->Phylum: Streptophyta
  -->Class: Equisetopsida
   -->Order: Gnetales
    -->Family: Gnetaceae
     -->Genus: Gnetum
      -->Species: Gnetum parvifolium
03. Combinatorial Therapeutic Effect(s)
Synergistic Effect
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Drug(s) whose efficacy can be enhanced by this phytochemical
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Combination Pair ID: 168
Pair Name Resveratrol, Temozolomide
Partner Name Temozolomide
Disease Info [ICD-11: 2F7Z] Glioma Investigative
Biological Phenomena Induction-->ROS-dependent AMPK-TSC-mTOR signaling pathway
Gene Regulation Up-regulation Expression BAX hsa581
Down-regulation Expression BCL2 hsa596
Up-regulation Expression CASP3 hsa836
Up-regulation Expression CASP7 hsa840
Up-regulation Expression CASP9 hsa842
Down-regulation Expression CCNB1 hsa891
Down-regulation Expression CDKN1A hsa1026
Down-regulation Expression LRRC59 hsa55379
Down-regulation Activity MAPK1 hsa5594
Down-regulation Activity MAPK14 hsa1432
Down-regulation Activity MAPK8 hsa5599
Up-regulation Phosphorylation TP53 hsa7157
In Vitro Model SHG-44 Astrocytoma Homo sapiens (Human) CVCL_6728
In Vivo Model SHG44 cells (5×10⁵ cells per mouse) in 5 μL of Hanks’ solution were injected intracranially into the right caudate nucleus of 6‐ to 8‐week‐old female nude mice using a screw guide technique as described
Result TMZ in combination with resveratrol remarkably increased reactive oxygen species (ROS) production, which serves as an upstream signal for AMP-activated protein kinase (AMPK) activation. Subsequently, activated AMPK inhibited mTOR signaling and downregulated antiapoptosis protein Bcl-2, which was contributed to the additive antiproliferation effects of combination treatment. In an orthotopic xenograft model of GBM, TMZ plus resveratrol treatment significantly reduced the volume of tumor, which was confirmed by decreased expression of Ki-67, a marker of proliferation index
Combination Pair ID: 264
Pair Name Resveratrol, Temozolomide
Partner Name Temozolomide
Disease Info [ICD-11: 2F7Z] Glioma Investigative
Biological Phenomena Inhibition-->Autophagy
Gene Regulation Down-regulation Expression MAP1LC3B hsa81631
Down-regulation Phosphorylation MAPK1 hsa5594
Up-regulation Cleavage PARP1 hsa142
In Vitro Model U-87MG ATCC Glioblastoma Homo sapiens (Human) CVCL_0022
In Vivo Model U87 MG cells in 0.1 ml MEM were subcutaneously (s.c.) injected into the right hind flank of the mice. Tumor sizes were measured with a caliper and were calculated as 1/2 × length × width2 in mm3. When the tumors grew to about 100 mm3, the tumor-bearing mice were randomly separated into treatment groups (n = 6/group).
Result TMZ-induced ROS/ERK-mediated autophagy protected glioma cells from apoptosis, and the combination of resveratrol with TMZ could improve the efficacy of chemotherapy for brain tumors.
Combination Pair ID: 368
Pair Name Resveratrol, ABT-737
Partner Name ABT-737
Disease Info [ICD-11: 2B33.3] Acute lymphoblastic leukemia Investigative
Biological Phenomena Induction-->DNA damage
Gene Regulation Up-regulation Expression BAX hsa581
Down-regulation Expression BCL2 hsa596
Up-regulation Expression TP53 hsa7157
In Vitro Model MOLT-4 Adult T acute lymphoblastic leukemia Homo sapiens (Human) CVCL_0013
Result The obtained data indicate that the combination of ABT-737 and resveratrol is a promising approach for acute lymphoblastic leukemia treatment that should be further explored.
Combination Pair ID: 369
Pair Name Resveratrol, Roscovitine
Partner Name Roscovitine
Disease Info [ICD-11: 2C60] Breast cancer Investigative
In Vitro Model MCF-7 Invasive breast carcinoma of no special type Homo sapiens (Human) CVCL_0031
Result We propose that resveratrol inactivates COX-1 by a "hit-and-run" mechanism, and offers a basis for the design of selective COX-1 inactivators that work through a mechanism-based event at the peroxidase active site.
Combination Pair ID: 372
Pair Name Resveratrol, BIBR1532
Partner Name BIBR1532
Disease Info [ICD-11: 2B90] Colon cancer Investigative
Gene Regulation Down-regulation Expression CCAT1 KEGG ID N.A.
Down-regulation Expression CRNDE KEGG ID N.A.
Down-regulation Expression PCAT1 KEGG ID N.A.
Down-regulation Expression PVT1 KEGG ID N.A.
Down-regulation Expression SNHG16 KEGG ID N.A.
In Vitro Model HT-29 Colon adenocarcinoma Homo sapiens (Human) CVCL_0320
Result Resveratrol, BIBR1532, or their combination may have anti-proliferative effect on colorectal cancer cells through repressing expression of LncRNAs that are involved in progression of CRC.
Combination Pair ID: 374
Pair Name Resveratrol, Talazoparib
Partner Name Talazoparib
Disease Info [ICD-11: 2C60] Breast cancer Investigative
Biological Phenomena Induction-->Blockade of cell cycle in G2/M phase
Gene Regulation Down-regulation Phosphorylation AKT1 hsa207
Up-regulation Expression ATG5 hsa9474
Up-regulation Expression ATG7 hsa10533
Down-regulation Expression HR hsa55806
Down-regulation Expression MAP1LC3A hsa84557
Down-regulation Expression MAP1LC3B hsa81631
Up-regulation Expression MAPK14 hsa1432
In Vitro Model MDA-MB-231 Breast adenocarcinoma Homo sapiens (Human) CVCL_0062
MCF-7 Invasive breast carcinoma of no special type Homo sapiens (Human) CVCL_0031
In Vivo Model Exponentially growing MCF-7 cells (5×10⁶ per mouse) were injected subcutaneously into the flank of 6 weeks old female SCID mice (weighing 25-35 g, 5 mice per group).
Result Resveratrol sensitizes breast cancer to PARP inhibitor, talazoparib through dual inhibition of AKT and autophagy flux
Combination Pair ID: 375
Pair Name Resveratrol, Cisplatin
Partner Name Cisplatin
Disease Info [ICD-11: 2B72] Gastric cancer Investigative
Biological Phenomena Induction-->Blockade of cell cycle in G2/M phase
Gene Regulation Up-regulation Activity ATF4 hsa468
Up-regulation Expression BAX hsa581
Down-regulation Expression BCL2 hsa596
Up-regulation Cleavage CASP12 hsa100506742
Down-regulation Expression CCNB1 hsa891
Down-regulation Expression CDC25C hsa995
Up-regulation Phosphorylation CDK1 hsa983
Up-regulation Activity CDKN1A hsa1026
Up-regulation Activity CDKN1B hsa1027
Up-regulation Expression DDIT3 hsa1649
Up-regulation Expression EIF2AK3 hsa9451
Up-regulation Phosphorylation EIF2S1 hsa1965
Up-regulation Expression HSPA5 hsa3309
Up-regulation Cleavage PARP1 hsa142
In Vitro Model AGS Gastric adenocarcinoma Homo sapiens (Human) CVCL_0139
Result These results indicated that RES is a promising adjuvant for DDP during GC chemotherapy.
Combination Pair ID: 376
Pair Name Resveratrol, Temozolomide
Partner Name Temozolomide
Disease Info [ICD-11: 2A00] Glioblastoma multiforme Investigative
Biological Phenomena Induction-->Apoptosis
Gene Regulation Down-regulation Expression BCL2 hsa596
Down-regulation Expression BIRC5 hsa332
Down-regulation Activity MGMT hsa4255
Down-regulation Phosphorylation STAT3 hsa6774
In Vitro Model RG2 Malignant glioma Rattus norvegicus (Rat) CVCL_3581
LN-18 Glioblastoma Homo sapiens (Human) CVCL_0392
LN-428 Glioblastoma Homo sapiens (Human) CVCL_3959
Result Our results demonstrated synergistic effects of Res/TMZ on RG-2 cells and their bilaterally sensitizing effects to LN-18 and LN-428 cells. Frequent upregulation of MGMT and activation of STAT3 are the unfavorable factors for the treatment of GBMs and they may be the potential targets of Res/TMZ therapy.
Combination Pair ID: 377
Pair Name Resveratrol, Docetaxel
Partner Name Docetaxel
Disease Info [ICD-11: 2C82] Prostate cancer Investigative
Biological Phenomena Induction-->Necroptosis
Gene Regulation Up-regulation Phosphorylation ATM hsa472
Up-regulation Phosphorylation ATR hsa545
Up-regulation Phosphorylation H2AX hsa3014
In Vitro Model LNCaP Prostate carcinoma Homo sapiens (Human) CVCL_0395
Result We report resveratrol as an adjuvant drug candidate for improving the outcome of treatment in DTX therapy. Although the underlying mechanisms of necroptosis should be investigated comprehensively, targeting apoptosis and necroptosis simultaneously in the treatment of cancer can be a useful strategy for the development of promising drug candidates.
Combination Pair ID: 378
Pair Name Resveratrol, Rapamycin
Partner Name Rapamycin
Disease Info [ICD-11: 2D10.1] Papillary thyroid cancer Investigative
Biological Phenomena Induction-->Apoptosis
Gene Regulation Down-regulation Phosphorylation AKT1 hsa207
Up-regulation Expression BAX hsa581
Down-regulation Expression BCL-xL hsa598
Up-regulation Expression CASP3 hsa836
Up-regulation Expression CASP8 hsa841
Up-regulation Expression CASP9 hsa842
Down-regulation Expression MCL1 hsa4170
Down-regulation Phosphorylation RPS6KB1 hsa6198
In Vitro Model KTC-1 Poorly differentiated thyroid gland carcinoma Homo sapiens (Human) CVCL_6300
TPC-1 Thyroid gland papillary carcinoma Homo sapiens (Human) CVCL_6298
In Vivo Model KTC-1 and TPC-1 cells in logarithmic growth phase were subcutaneously inoculated into the right armpit of nude mice (5×10⁶ cells/mouse).
Result The present study suggests that the combination of rapamycin and resveratrol may be a promising strategy for the treatment of papillary thyroid cancer.
Combination Pair ID: 379
Pair Name Resveratrol, Olaparib
Partner Name Olaparib
Disease Info [ICD-11: 2C60] Breast cancer Investigative
Biological Phenomena Induction-->DNA damage
Gene Regulation Up-regulation Expression BAX hsa581
Down-regulation Expression BCL-xL hsa598
Down-regulation Expression BRCA1 hsa672
Down-regulation Expression PARP1 hsa142
In Vitro Model MCF-7 Invasive breast carcinoma of no special type Homo sapiens (Human) CVCL_0031
T-47D Invasive breast carcinoma of no special type Homo sapiens (Human) CVCL_0553
In Vivo Model Tumor was induced by injecting MCF-7 cells (1 × 107 in 200 μL sterile 1X PBS) on the right breast fat pads of 6–7 weeks old female BALB/c mice. After formation of tumor, the mice were orally treated with RES + OLA combination (40 mg/kg RES and 20 nM/kg OLA per day) for 30 days.
Result RES + OLA combination treatment enhanced breast cancer cell death by causing excessive DNA damage and also simultaneously inhibiting the HR pathway.
Combination Pair ID: 380
Pair Name Resveratrol, Gemcitabine
Partner Name Gemcitabine
Disease Info [ICD-11: 2C10] Pancreatic cancer Investigative
Biological Phenomena Induction-->Apoptosis
Gene Regulation Up-regulation Phosphorylation GSK3B hsa2932
Down-regulation Expression VEGFA hsa7422
In Vitro Model Capan-2 Pancreatic ductal adenocarcinoma Homo sapiens (Human) CVCL_0026
MIA PaCa-2 Pancreatic ductal adenocarcinoma Homo sapiens (Human) CVCL_0428
PANC-1 Pancreatic ductal adenocarcinoma Homo sapiens (Human) CVCL_0480
In Vivo Model 5×10⁶ MiaPaCa2 cells were suspended in DMEM medium and transplanted subcutaneously in each nude mouse.
Result These results suggest that VEGF-B signaling pathway plays an important role in the development of PaCa and combination of GEM and RSV would be a promising modality for clinical PaCa therapy.
Combination Pair ID: 381
Pair Name Resveratrol, Cisplatin
Partner Name Cisplatin
Disease Info [ICD-11: 2C60] Breast cancer Investigative
Biological Phenomena Induction-->Apoptosis
Gene Regulation Up-regulation Activity CASP3 hsa836
Up-regulation Activity CASP9 hsa842
In Vitro Model MDA-MB-231 Breast adenocarcinoma Homo sapiens (Human) CVCL_0062
Result RSV, an effective anti-oxidant, and CDDP as an effective drug in cancer treatment, were found to increase apoptosis when given in the MDA-MB-231 cell.
Combination Pair ID: 382
Pair Name Resveratrol, Temozolomide
Partner Name Temozolomide
Disease Info [ICD-11: 2A00] Glioblastoma multiforme Investigative
Biological Phenomena Induction-->Apoptosis
Gene Regulation Down-regulation Expression MGMT hsa4255
Up-regulation Expression PIAS3 hsa10401
Up-regulation Expression PTPN11 hsa5781
Up-regulation Expression PTPN6 hsa5777
Up-regulation Expression SOCS3 hsa9021
Down-regulation Expression STAT3 hsa6774
In Vitro Model A-172 Glioblastoma Homo sapiens (Human) CVCL_0131
LN-428 Glioblastoma Homo sapiens (Human) CVCL_3959
Result Res inhibited STAT3 signaling through modulation of PIAS3, SHP1, SHP2, and SOCS3, thereby attenuating tumor growth and increasing sensitivity to TMZ. Therefore, Res is an ideal candidate to be used in TMZ combined chemotherapy for GBM.
Combination Pair ID: 383
Pair Name Resveratrol, TNF-related apoptosis inducing ligand
Partner Name TNF-related apoptosis inducing ligand
Disease Info [ICD-11: 2C90.0] Renal cell carcinoma Investigative
Biological Phenomena Induction-->Apoptosis
Gene Regulation Up-regulation Activity CASP3 hsa836
Up-regulation Activity CASP8 hsa841
Up-regulation Activity CASP9 hsa842
Down-regulation Expression XIAP hsa331
In Vitro Model 786-O Renal cell carcinoma Homo sapiens (Human) CVCL_1051
OS-RC-2 Clear cell renal cell carcinoma Homo sapiens (Human) CVCL_1626
In Vivo Model These data demonstrated that RES plus Ad5/35-TRAIL significantly inhibited RCC xenograft growth in nude mice.
Result Our data demonstrated that RES plus Ad5/35-TRAIL significantly inhibited RCC xenograft growth in nude mice. These results suggest the possibility of a new combination therapeutic leading to the improvement of RCC treatment.
Combination Pair ID: 808
Pair Name Resveratrol, Celecoxib
Partner Name Celecoxib
Disease Info [ICD-11: 2C60] Breast cancer Investigative
Gene Regulation Down-regulation Expression COX2 hsa4513
In Vitro Model MCF-7 Invasive breast carcinoma of no special type Homo sapiens (Human) CVCL_0031
In Vivo Model Mammary carcinogenesis was initiated with two intra peritoneal doses (50 mg/kg body weight each) of N-methyl-N-nitrosourea (NMU) dissolved in a physiological NaCl solution.
Result This study showed that in NMU-induced mammary cancer in rats, the combination of resveratrol and celecoxib led to a significant reduction in all tumor parameters. In addition, in terms of tumor volume, the combination was more efficient than celecoxib as a single agent.
Combination Pair ID: 809
Pair Name Resveratrol, Flutamide
Partner Name Flutamide
Disease Info [ICD-11: 2C82] Prostate cancer Investigative
Gene Regulation Down-regulation Expression AR hsa367
In Vitro Model LNCaP Prostate carcinoma Homo sapiens (Human) CVCL_0395
PC-3 Prostate carcinoma Homo sapiens (Human) CVCL_0035
DU145 Prostate carcinoma Homo sapiens (Human) CVCL_0105
Result Resveratrol works in concert with antiandrogen flutamide to reduce the amount and activity of AR, suggesting new therapeutic strategies for the treatment of PCa.
Combination Pair ID: 810
Pair Name Resveratrol, Trastuzumab
Partner Name Trastuzumab
Disease Info [ICD-11: 2C60] Breast cancer Investigative
Biological Phenomena Induction-->Blockade of cell cycle in G2/M phase
Gene Regulation Down-regulation Expression BCL2 hsa596
Down-regulation Expression ERBB2 hsa2064
In Vitro Model MCF-7 Invasive breast carcinoma of no special type Homo sapiens (Human) CVCL_0031
T-47D Invasive breast carcinoma of no special type Homo sapiens (Human) CVCL_0553
Result Herceptin/resveratrol and herceptin/didox combinations improved the cytotoxic profile of herceptin in both T47D and MCF-7 breast cancer cell lines.
Combination Pair ID: 812
Pair Name Resveratrol, Sorafenib
Partner Name Sorafenib
Disease Info [ICD-11: 2C90.0] Renal cell carcinoma Investigative
Gene Regulation Down-regulation Phosphorylation AKT1 hsa207
Up-regulation Expression BAX hsa581
Down-regulation Expression BCL2 hsa596
Down-regulation Expression HIF1A hsa3091
Down-regulation Phosphorylation MAPK1 hsa5594
Down-regulation Phosphorylation MEK1 hsa5604
Down-regulation Phosphorylation MTOR hsa2475
Down-regulation Phosphorylation RAF1 hsa5894
Down-regulation Phosphorylation RPS6KB1 hsa6198
Down-regulation Expression VEGFA hsa7422
In Vitro Model RenCa Mouse kidney carcinoma Mus musculus (Mouse) CVCL_2174
HEK293T Healthy Homo sapiens (Human) CVCL_0063
In Vivo Model After reaching the required number of cells, the cells were harvested, washed and appropriate amount of PBS was added to prepare Renca cell suspension at a concentration of 5×10⁷ cells/mL. 0.2 mL was injected into the armpit of each mouse, and weighed and grouped the next day.
Result PEGylated resveratrol combined with sorafenib can achieve synergistic anti-RCC activity, and the mechanism may be related to the inhibition of Akt/mTOR/p70S6k-4EBP-1 and c-Raf7MEK/ERK signaling pathways.
Combination Pair ID: 813
Pair Name Resveratrol, Cisplatin
Partner Name Cisplatin
Disease Info [ICD-11: 2C73] Ovarian cancer Investigative
Biological Phenomena Induction-->Blockade of cell cycle in S phase
Gene Regulation Up-regulation Phosphorylation AKT1 hsa207
Up-regulation Cleavage CASP3 hsa836
Up-regulation Cleavage CASP9 hsa842
Down-regulation Expression CCNA2 hsa890
Down-regulation Expression CCNB1 hsa891
Down-regulation Phosphorylation MAPK14 hsa1432
Up-regulation Phosphorylation MAPK8 hsa5599
Up-regulation Cleavage PARP1 hsa142
In Vitro Model SK-OV-3 Ovarian serous cystadenocarcinoma Homo sapiens (Human) CVCL_0532
Result Resveratrol Enhances Cytotoxic Effects of Cisplatin by Inducing Cell Cycle Arrest and Apoptosis in Ovarian Adenocarcinoma SKOV-3 Cells through Activating the p38 MAPK and Suppressing AKT
Drug(s) whose toxicity can be decreased by this phytochemical
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Combination Pair ID: 373
Pair Name Resveratrol, Cisplatin
Partner Name Cisplatin
Disease Info [ICD-11: 2B72] Gastric cancer Investigative
Biological Phenomena Induction-->Blockade of cell cycle in G0/G1 phase
Gene Regulation Up-regulation Expression CDKN1A hsa1026
Up-regulation Expression CDKN2A hsa1029
Down-regulation Expression IL1B hsa3553
Down-regulation Expression IL6 hsa3569
Up-regulation Expression MAPK14 hsa1432
Down-regulation Expression MMP2 hsa4313
Down-regulation Expression TNF hsa7124
Up-regulation Expression TP53 hsa7157
In Vitro Model AGS Gastric adenocarcinoma Homo sapiens (Human) CVCL_0139
Result Combination therapy of cisplatin and resveratrol to induce cellular aging in gastric cancer cells: Focusing on oxidative stress, and cell cycle arrest
Combination Pair ID: 811
Pair Name Resveratrol, Sirolimus
Partner Name Sirolimus
Disease Info [ICD-11: 2F7C] Lymphangioleiomyomatosis Investigative
Gene Regulation Down-regulation Expression VEGFD KEGG ID N.A.
Result The addition of resveratrol was safe and well tolerated in patients with lymphangioleiomyomatosis receiving sirolimus and was associated with modest improvement in HRQOL. Larger controlled trials of this combination may be warranted to assess definitively the usefulness of resveratrol as an additive therapy in lymphangioleiomyomatosis.
04. Reference
No. Title Href
1 Combination therapy of cisplatin and resveratrol to induce cellular aging in gastric cancer cells: Focusing on oxidative stress, and cell cycle arrest. Front Pharmacol. 2023;13:1068863. Published 2023 Jan 4. doi:10.3389/fphar.2022.1068863. Click
2 Safety and Efficacy of Combined Resveratrol and Sirolimus in Lymphangioleiomyomatosis. Chest. 2023;163(5):1144-1155. doi:10.1016/j.chest.2023.01.007. Click
3 Resveratrol enhances the antitumor effects of temozolomide in glioblastoma via ROS-dependent AMPK-TSC-mTOR signaling pathway. CNS Neurosci Ther. 2012;18(7):536-546. doi:10.1111/j.1755-5949.2012.00319.x Click
4 Resveratrol enhances the therapeutic effect of temozolomide against malignant glioma in vitro and in vivo by inhibiting autophagy. Free Radic Biol Med. 2012;52(2):377-391. doi:10.1016/j.freeradbiomed.2011.10.487 Click
5 Combination of ABT-737 and resveratrol enhances DNA damage and apoptosis in human T-cell acute lymphoblastic leukemia MOLT-4 cells. Toxicol In Vitro. 2017 Aug;42:38-46. doi: 10.1016/j.tiv.2017.03.013. Click
6 Resveratrol is a peroxidase-mediated inactivator of COX-1 but not COX-2: a mechanistic approach to the design of COX-1 selective agents. J Biol Chem. 2004 May 21;279(21):22727-37. doi: 10.1074/jbc.M314302200. Click
7 Combination of resveratrol and BIBR1532 inhibits proliferation of colon cancer cells by repressing expression of LncRNAs. Med Oncol. 2021 Nov 15;39(1):12. doi: 10.1007/s12032-021-01611-w. Click
8 Resveratrol sensitizes breast cancer to PARP inhibitor, talazoparib through dual inhibition of AKT and autophagy flux. Biochem Pharmacol. 2022 May;199:115024. doi: 10.1016/j.bcp.2022.115024. Click
9 Resveratrol synergizes with cisplatin in antineoplastic effects against AGS gastric cancer cells by inducing endoplasmic reticulum stress‑mediated apoptosis and G2/M phase arrest. Oncol Rep. 2020 Oct;44(4):1605-1615. doi: 10.3892/or.2020.7708. Click
10 Synergistic Effects of Resveratrol and Temozolomide Against Glioblastoma Cells: Underlying Mechanism and Therapeutic Implications. Cancer Manag Res. 2020 Sep 11;12:8341-8354. doi: 10.2147/CMAR.S258584. Click
11 Synergistic anticancer activity of resveratrol in combination with docetaxel in prostate carcinoma cells. Nutr Res Pract. 2021 Feb;15(1):12-25. doi: 10.4162/nrp.2021.15.1.12. Click
12 Resveratrol potentiates the anti-tumor effects of rapamycin in papillary thyroid cancer: PI3K/AKT/mTOR pathway involved. Arch Biochem Biophys. 2020 Aug 15;689:108461. doi: 10.1016/j.abb.2020.108461. Click
13 Olaparib enhances the Resveratrol-mediated apoptosis in breast cancer cells by inhibiting the homologous recombination repair pathway. Exp Cell Res. 2022 Nov 1;420(1):113338. doi: 10.1016/j.yexcr.2022.113338. Click
14 Gemcitabine potentiates anti-tumor effect of resveratrol on pancreatic cancer via down-regulation of VEGF-B. J Cancer Res Clin Oncol. 2021 Jan;147(1):93-103. doi: 10.1007/s00432-020-03384-7. Click
15 Resveratrol increases the sensitivity of breast cancer MDA-MB-231 cell line to cisplatin by regulating intrinsic apoptosis. Iran J Basic Med Sci. 2021 Jan;24(1):66-72. doi: 10.22038/ijbms.2020.50485.11501. Click
16 Resveratrol Enhances Temozolomide Efficacy in Glioblastoma Cells through Downregulated MGMT and Negative Regulators-Related STAT3 Inactivation. Int J Mol Sci. 2023 May 29;24(11):9453. doi: 10.3390/ijms24119453. Click
17 Mechanism and therapeutic prospect of resveratrol combined with TRAIL in the treatment of renal cell carcinoma. Cancer Gene Ther. 2020 Aug;27(7-8):619-623. doi: 10.1038/s41417-019-0150-6. Click
18 Resveratrol enhances the chemopreventive effect of celecoxib in chemically induced breast cancer in rats. Eur J Cancer Prev. 2014 Nov;23(6):506-13. doi: 10.1097/CEJ.0000000000000083. Click
19 Combination of resveratrol and antiandrogen flutamide has synergistic effect on androgen receptor inhibition in prostate cancer cells. Anticancer Res. 2011;31(10):3323-3330. Click
20 The chemomodulatory effects of resveratrol and didox on herceptin cytotoxicity in breast cancer cell lines. Sci Rep. 2015 Jul 9;5:12054. doi: 10.1038/srep12054. Click
21 Synergistic anti-tumour activity of sorafenib in combination with pegylated resveratrol is mediated by Akt/mTOR/p70S6k-4EBP-1 and c-Raf7MEK/ERK signaling pathways. Heliyon. 2023 Aug 19;9(8):e19154. doi: 10.1016/j.heliyon.2023.e19154. Click
22 Resveratrol Enhances Cytotoxic Effects of Cisplatin by Inducing Cell Cycle Arrest and Apoptosis in Ovarian Adenocarcinoma SKOV-3 Cells through Activating the p38 MAPK and Suppressing AKT. Pharmaceuticals (Basel). 2023 May 17;16(5):755. doi: 10.3390/ph16050755. Click
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