4.7 Article

Curcuminoids Suppress the Growth of Pharynx and Nasopharyngeal Carcinoma Cells through Induced Apoptosis

Journal

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
Volume 57, Issue 9, Pages 3765-3770

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jf803758x

Keywords

Curcuminoids; nasopharyngeal carcinoma (NPC); apoptosis

Ask authors/readers for more resources

Nasopharyngeal carcinoma (NPC) is one of the common malignant cancers in China, and radiotherapy or chemotherapy is the main therapy method for NPC. Curcuminoids (or curcumin), natural antioxidants, have been recently shown to produce a potent chemopreventive action against several types of cancer. They have also displayed antioxidant and anti-inflammatory activities. In the present study, the antiproliferation and induced apoptosis effects of curcuminoids have been investigated in Detroit 562 cells (human pharynx carcinoma) and HONE-1 (human nasopharyngeal carcinoma) cells. Results indicated that curcuminoids have produced an inhibition of cell proliferation as well as the activation of apoptosis in these cancer cells. Both effects were observed to increase in proportion with the dose of curcuminoids. The DNA fragmentation, caspase-3 activation,and NF-kappa B transcriptional factor activity have been studied. By these approaches, apoptosis was induced by curcuminoids in the pharynx and nasopharyngeal cancer cells via caspase-3-dependent pathway. However, a different dependency has been observed, whereas proliferation inhibition and apoptosis depend upon the amount of curcuminoid treatment in the cancer cells.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Article Cell Biology

Simvastatin induces G(1) arrest by up-regulating GSK3 and down-regulating CDK4/cyclin D1 and CDK2/cyclin E1 in human primary colorectal cancer cells

Ming-Jenn Chen, An-Ching Cheng, Ming-Fen Lee, Yi-Chiang Hsu

JOURNAL OF CELLULAR PHYSIOLOGY (2018)

Article Genetics & Heredity

Pre-treatment with angiotensin-(1-7) inhibits tumor growth via autophagy by downregulating PI3K/Akt/mTOR signaling in human nasopharyngeal carcinoma xenografts

Yu-Tsai Lin, Hung-Chen Wang, Hui-Ching Chuang, Yi-Chiang Hsu, Ming-Yu Yang, Chih-Yen Chien

JOURNAL OF MOLECULAR MEDICINE-JMM (2018)

Article Cell Biology

The effects of cucurbitacin E on GADD45β-trigger G2/M arrest and JNK-independent pathway in brain cancer cells

An-Chin Cheng, Yi-Chiang Hsu, Chiang-Chin Tsai

JOURNAL OF CELLULAR AND MOLECULAR MEDICINE (2019)

Article Chemistry, Medicinal

Sulforaphane Decrease of SERTAD1 Expression Triggers G1/S Arrest in Breast Cancer Cells

An-Chin Cheng, Ching-Ju Shen, Chao-Ming Hung, Yi-Chiang Hsu

JOURNAL OF MEDICINAL FOOD (2019)

Article Biotechnology & Applied Microbiology

Therapeutic Potential of RTA 404 in Human Brain Malignant Glioma Cell Lines via Cell Cycle Arrest via p21/AKT Signaling

Tai-Hsin Tsai, Ann-Shung Lieu, Yi-Wen Wang, Sheau-Fang Yang, Yi-Chiang Hsu, Chih-Lung Lin

Summary: RTA 404 can significantly inhibit the proliferation, cell motility, cell cycle progression, and induce apoptosis in GBM cells in vitro. Furthermore, it may exert its effects by inhibiting N-cadherin and E-cadherin expression.

BIOMED RESEARCH INTERNATIONAL (2021)

Article Biochemistry & Molecular Biology

Novel Aptamer-Based Small-Molecule Drug Screening Assay to Identify Potential Sclerostin Inhibitors against Osteoporosis

Chien-Ching Lee, Chao-Ming Hung, Chung-Hwan Chen, Yi-Chiang Hsu, Yuan-Pin Huang, Tsung-Bin Huang, Mon-Juan Lee

Summary: A novel aptamer-based competitive drug screening platform was developed for osteoporosis, facilitating high-throughput screening for potential small-molecule sclerostin inhibitors and offering a reliable strategy for target-specific new drug discovery. The potential sclerostin inhibitors obtained in this study showed promising effects on decreasing sclerostin levels and increasing alkaline phosphatase activity in osteocyte and mesenchymal stem cells, suggesting their potential as new therapeutics for osteoporosis.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2021)

Article Pharmacology & Pharmacy

Induction of Mitosis Delay and Apoptosis by CDDO-TFEA in Glioblastoma Multiforme

Tai-Hsin Tsai, Ann-Shung Lieu, Tzuu-Yuan Huang, Aij-Lie Kwan, Chih-Lung Lin, Yi-Chiang Hsu

Summary: CDDO-TFEA can inhibit proliferation, cell cycle progression, and induce apoptosis in GBM cells, possibly through its inhibition of Cyclin B1, CDK1 expression, and Cyclin B1/CDK1 association, as well as the promotion of CHK1 and CHK2 expression.

FRONTIERS IN PHARMACOLOGY (2021)

Article Medicine, General & Internal

RTA404, an Activator of Nrf2, Activates the Checkpoint Kinases and Induces Apoptosis through Intrinsic Apoptotic Pathway in Malignant Glioma

Tai-Hsin Tsai, Ann-Shung Lieu, Tzuu-Yuan Huang, Aij-Lie Kwan, Chih-Lung Lin, Yi-Chiang Hsu

Summary: RTA404 significantly inhibited cell viability and induced apoptosis in the U87MG cell line. Flow cytometry analysis revealed a significant decrease in mitochondrial membrane potential and an increase in apoptotic cell percentage with RTA404 treatment. Additionally, RTA404 may activate the DNA damage checkpoint system and induce apoptosis in established U87MG cells.

JOURNAL OF CLINICAL MEDICINE (2021)

Article Biochemistry & Molecular Biology

NAMPT Inhibitor and P73 Activator Represses P53 R175H Mutated HNSCC Cell Proliferation in a Synergistic Manner

Bi-He Cai, Zhi-Yu Bai, Ching-Feng Lien, Si-Jie Yu, Rui-Yu Lu, Ming-Han Wu, Wei-Chen Wu, Chia-Chi Chen, Yi-Chiang Hsu

Summary: The aggregation of mutant p53 induces its gain-of-function in head and neck squamous cell carcinoma. A combination therapy involving an NAMPT inhibitor and a p73 activator effectively suppresses the growth of cells with p53 gain-of-function mutants.

BIOMOLECULES (2022)

Article Biochemistry & Molecular Biology

PTC124 Rescues Nonsense Mutation of Two Tumor Suppressor Genes NOTCH1 and FAT1 to Repress HNSCC Cell Proliferation

Ming-Han Wu, Rui-Yu Lu, Si-Jie Yu, Yi-Zhen Tsai, Ying-Chen Lin, Zhi-Yu Bai, Ruo-Yu Liao, Yi-Chiang Hsu, Chia-Chi Chen, Bi-He Cai

Summary: This study found that PTC124 can induce the expression of tumor suppressor genes NOTCH1 and FAT1 in head and neck squamous cell carcinoma, inhibiting cell proliferation and showing therapeutic potential.

BIOMEDICINES (2022)

Article Biochemistry & Molecular Biology

RTA dh404 Induces Cell Cycle Arrest, Apoptosis, and Autophagy in Glioblastoma Cells

Tai-Hsin Tsai, Yu-Feng Su, Cheng-Yu Tsai, Chieh-Hsin Wu, Kuan-Ting Lee, Yi-Chiang Hsu

Summary: RTA dh404 is a novel synthetic oleanolic acid derivative with various properties and therapeutic effects on cancers. It reduces glioma cell viability and induces apoptosis, autophagy, and cell cycle arrest in glioblastoma cells. These effects are mediated by the regulation of associated genes, indicating the potential of RTA dh404 as a drug candidate for glioblastoma treatment.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2023)

Article Biochemistry & Molecular Biology

Sulforaphane-Induced Cell Mitotic Delay and Inhibited Cell Proliferation via Regulating CDK5R1 Upregulation in Breast Cancer Cell Lines

Chao-Ming Hung, Tai-Hsin Tsai, Kuan-Ting Lee, Yi-Chiang Hsu

Summary: Our research shows that sulforaphane (SFN) has chemopreventive and potential chemotherapeutic effects on breast adenocarcinoma. Further studies are needed to understand the mechanisms behind SFN's antitumor activity. Our experiments demonstrate that SFN inhibits the growth of cancer cells and induces apoptosis, suggesting it could be used as an anticancer agent.

BIOMEDICINES (2023)

Article Chemistry, Medicinal

A Novel Synthetic Oleanolic Acid Derivative Inhibits Glioma Cell Proliferation by Regulating Cell Cycle G2/M Arrest

Tai-Hsin Tsai, Cheng-Yu Tsai, Sin-Hua Moi, Chieh-Hsin Wu, Kuan-Ting Lee, Yi-Chiang Hsu, Yu-Feng Su

Summary: CDDO-dhTFEA has anticancer effects on glioblastoma cells by reducing cell proliferation and regulating cell cycle proteins. It induces G2/M cell cycle arrest and inhibits proliferation in U87MG and GBM8401 cells.

PHARMACEUTICALS (2023)

Article Cell Biology

Cyclophosphamide promotes breast cancer cell migration through CXCR4 and matrix metalloproteinases

Chao-Ming Hung, Yi-Chiang Hsu, Tzu-Yu Chen, Chi-Chang Chang, Mon-Juan Lee

CELL BIOLOGY INTERNATIONAL (2017)

Article Cell Biology

Inducement of apoptosis by cucurbitacin E, a tetracyclic triterpenes, through death receptor 5 in human cervical cancer cell lines

Ya-Min Cheng, Ching-Ju Shen, Chi-Chang Chang, Cheng-Yang Chou, Ching-Chou Tsai, Yi-Chiang Hsu

CELL DEATH DISCOVERY (2017)

No Data Available