New ‘nanodrug’ can attack breast cancer cells from the inside outMarch 30th, 2011 - 3:18 pm ICT by ANI
Washington, Mar 30 (ANI): Researchers at Cedars-Sinai’s Maxine Dunitz Neurosurgical Institute have developed a new nanodrug that breaks down barriers to attack breast cancer cells from the inside out.
Unlike other drugs that target cancer cells from the outside with minimal effect, this therapy consists of multiple drugs chemically bonded to a ‘transport vehicle’.
This ‘transport vehicle’ spares healthy cells, accumulates inside tumour cells and attacks molecular targets that enable cancer cells to grow and spread.
Studies using a mouse model showed this highly targeted approach, using combinations of drugs, to be more effective than standard treatment methods.
Researchers targeted HER2-positive breast cancer - a type that, due to a genetic mutation, makes excessive amounts of a protein that promotes the growth of cancer cells.
One commonly used antitumor drug, trastuzumab (Herceptin), is sometimes beneficial, but with advantages and disadvantages.
It is an antibody to the HER2 antigen, which means it naturally seeks out this protein in cancers.
The researchers reported in their recent studies that the new drug carried multiple molecular components, each with a distinct role.
These key components included: Herceptin to target the existing HER2 protein; another molecule to attack a genetic mechanism responsible for the production of new protein; and a molecule to open tumor blood vessels and deliver the drugs into the cancer cells for release.
Injected into mice with implanted human breast cancer cells, the drugs accumulated in the cancer cells and worked together to significantly reduce tumour growth.
The drug is in an emerging class called nanobiopolymeric conjugates, or nanoconjugates.
“Nanobiopolymers enhance cancer cell targeting and treatment in several ways: Certain antibodies can be attached to precisely target proteins in tumor cells; drug resistance and systemic side-effects are reduced because drugs are ‘bound’ to the platform and delivered to the interior of cancer cells without affecting healthy cells; and multiple drugs can be carried on a single platform, making it possible to simultaneously attack several targets,” said senior author Julia Y. Ljubimova.
“Based on our studies, our nanobioconjugate appears to be a safe and efficient delivery platform that may be tailored to treat a wide array of disorders. It is harmlessly degraded to carbon dioxide and water, nontoxic to normal tissue, and, unlike some drugs, it is non-immunogenic, meaning it does not stimulate the immune system to the point of causing allergic reactions, which may range from mild coughs or rashes to sudden, life-threatening symptoms,” she added.
The findings appear in the recent issue of Cancer Research. (ANI)
- Soon, a 'nano drug' jab that hits brain tumour's bullseye - Nov 06, 2010
- Combo therapy may overcome Herceptin-resistant breast cancer - Mar 14, 2011
- New potential target for breast cancer therapy identified - Dec 23, 2010
- Erectile dysfunction drug could enhance delivery of herceptin to brain tumours - May 08, 2010
- Silica cages help anti-cancer antibodies prevent tumour growth in mice - May 22, 2010
- Overabundance of protein promotes growth of breast cancer stem cells - Feb 16, 2011
- 'Wonderdrug' keeps breast cancer away - Feb 25, 2011
- Silencing 'hedgehog' molecule halts cancer - Jun 06, 2011
- Light sensitive drugs to target cancer - Jun 05, 2011
- Biophysicist attempts to block protein to prevent breast, prostate cancer - Apr 20, 2011
- New hope for cancer cure - Jul 08, 2011
- Super vaccine could knock out 70 percent of cancers - Dec 13, 2011
- Compound used to control cholesterol may also kill breast cancer - Feb 23, 2011
- Normal healthy breast cells can help kill cancer cells - Apr 14, 2011
- Genetic pathways involved in breast cancer identified - Mar 04, 2011
Tags: breast cancer, breast cancer cells, cancer cell, distinct role, drug resistance, dunitz, genetic mechanism, genetic mutation, her2 protein, herceptin, human breast cancer, maxine dunitz neurosurgical institute, minimal effect, molecular components, molecular targets, systemic side effects, target cancer cells, tumor blood vessels, tumor cells, tumour cells