AMMONIUM TETRATHIOMOLYBDATE
- Molecular Formula: H8N2M0S4
- Molecular Weight: 260.28 g/mol
- Sequence: Non-Peptide
DESCRIPTION
Ammonium tetrathiomolybdate (TM) was developed as a non-toxic treatment for Wilson’s disease, which is a condition that results in copper buildup in the body. Tetrathiomolybdate binds both food copper and endogenously produced copper and prevents their absorption when taken with food. When taken without food it enters the blood and binds with available copper to prevent it being used by cells. Tetrathiomolybdate has also shown to be a promising treatment for cancer. Copper is involved in turning on the growth of new blood vessels that tumors depend on for growth. By depriving the tumors of the copper supply that is needed for new blood vessels, the growth may be slowed or stabilized. It has also been shown to target the copper transporter ATP7A and enhance the sensitivity of breast cancer to Cisplatin treatment, as well as, decreasing the development of resistance to cisplatin.
PROTOCOL
- Content & Potency: 40mg capsules provided in a quantity of 90.
- Suggested dosage: Take one capsule by mouth three times daily between meals.
CLINICAL RESEARCH
Ammonium tetrathiomolybdate treatment targets the copper transporterATP7A and enhances sensitivity of breast cancer to cisplatin
CristineL. Chisholm, #2 Haitao Wang, #1 Ada Hang-Heng Wong, 1 GuelaguetzaVazquez-Ortiz, 2 Weiping Chen, 3 Xiaoling Xu, 1 and Chu-Xia Deng 1,2
Abstract
Cisplatin is an effective breast cancer drug but resistance often develops over prolonged chemotherapy. Therefore, we performed a candidate approach RNAi screen in combination with cisplatin treatment to identify molecular pathways conferring survival advantages. The screen identified ATP7A as a therapeutic target. ATP7A is a copper ATPase transporter responsible for intercellular movement and sequestering of cisplatin. Pharmaceutical replacement for ATP7A by ammonium tetrathiomolybdate (TM) enhanced cisplatin treatment in breast cancer cells. Allograft and xenograft models in athymic nude mice treated with cisplatin/TM exhibited retarded tumor growth, reduced accumulation of cancer stem cells and decreased cell proliferation as compared to mono-treat – ment with cisplatin or TM. Cisplatin/TM treatment of cisplatin- resistant tumors reduced ATP7A protein levels, attenuated cisplatin sequestering by ATP7A, increased nuclear availability of cisplatin, and subsequently enhanced DNA damage and apoptosis. Microarray analysis of gene ontology pathways that responded uniquely to cisplatin/ TM double treatment depicted changes in cell cycle regulation, specifically in the G1/S transition. These findings offer the potential to combat platinum-resistant tumors and sensitize patients to conventional breast cancer treatment by identifying and targeting the resistant tumors’ unique molecular adaptations.
Here are some reliable sources for information on Ammonium Tetrathiomolybdate:
- Wikipedia: The Wikipedia article on Ammonium Tetrathiomolybdate provides an overview of the chemical, its properties, and its applications. Link: https://en.wikipedia.org/wiki/Ammonium_tetrathiomolybdate
- ScienceDirect: ScienceDirect is a scientific database that provides research papers, books and reference material on various topics, including Ammonium Tetrathiomolybdate. Link: https://www.sciencedirect.com/topics/chemistry/ammonium-tetrathiomolybdate –
These resources should provide you with a good starting point for your research on Ammonium Tetrathiomolybdate. However, always remember to double-check and verify the information you find from multiple sources to ensure accuracy and reliability.
AMMONIUM TETRATHIOMOLYBDATE Research
Here are some examples of research studies that have been conducted on the peptide AMMONIUM TETRATHIOMOLYBDATE:
- A study on the synthesis, characterization, and antitumor activity of AMMONIUM TETRATHIOMOLYBDATE nanoparticles: https://www.ncbi.nlm.nih.gov/pubmed/31061812
- A research article describing the potential use of AMMONIUM TETRATHIOMOLYBDATE as an antibacterial agent: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830109/
- A study on the role of AMMONIUM TETRATHIOMOLYBDATE in inhibiting copper corrosion: https://www.sciencedirect.com/science/article/pii/S0300944014004343
- A review article on the use of AMMONIUM TETRATHIOMOLYBDATE in catalysis: https://www.sciencedirect.com/science/article/pii/S0162013419304064
- A research article on the potential of AMMONIUM TETRATHIOMOLYBDATE as a therapeutic agent for treating copper accumulation disorders: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5683891/
Please note that this is not an exhaustive list and there may be other studies that have been conducted on AMMONIUM TETRATHIOMOLYBDATE.
POPULAR
Peptide pages
AMMONIUM
AMMONIUM Molecular Formula: H8N2M0S4 Molecular Weight: 260.28 g/mol Sequence: Non-Peptide DESCRIPTION Ammonium tetrathiomolybdate (TM) was developed as a non-toxic treatment for Wilson’s disease, which is
IPAMORELIN
IPAMORELIN GROWTH HORMONESECRETAGOGUE PEPTIDE Molecular Formula:C38H49N9O5 Molecular Weight: 711.863 Sequence: Aib-His-D-2-Nal-D-Phe-Lys-NH DESCRIPTION Ipamorelin is a selective GH-Secretagogue and ghrelin receptor agonist. The potency of ghrelin
i RGD
i RGD CANCER TARGETING PEPTIDE Molecular Formula: C 35 H 58 N 14 O 13 S 2 Molecular Weight: 947.07g/mol Sequence: Cys-Arg-Gly-Asp-Lys- Gly-Pro-Asp-Cys DESCRIPTION iRGD