In the Sixties hippies turned on with marijuana. In the very near future they may be using the same plant to turn off.
Turn off the bad gene that promotes the spread of aggressive breast cancer that is!
Sean McAllister, Ph.D., and Pierre Desprez, Ph.D. at California Pacific Medical Center Research Institute in San Francisco have been testing cannabidiol.
We discovered that cannabidiol (CBD), a non-psychotropic compound from the plant Cannabis sativa, can inhibit the processes that allow breast cancer cells to grow and spread (metastasis). The mechanism that would explain the inhibitory action of CBD in vivo (in a living organism) on breast cancer metastasis has not been elucidated. CBD is a novel inhibitor of a gene whose activity is intimately linked to the aggressiveness of human breast cancers; this gene has been termed Id-1.
Using cultures of breast cancer cells, we discovered that Id-1 was a key gene whose expression needed to be reduced in order for CBD to inhibit the spread of breast cancer.
About 40% of the cannabis plant is the compound cannabidiol. It does not contain THC.
The study is funded by the National Institutes of Health. Early test results on animals are very positive. The doctors hope to begin testing cannabidiol on humans within 2-3 years.
An important goal among breast cancer advocates is to find non-toxic therapies that specifically target metastatic breast cancer and not healthy tissues. Our targeted approach is expected to satisfy these criteria.
Additionally, due to the difficulties in accessing efficient screening methods, metastatic breast cancer is more likely to be diagnosed in women with poor social conditions. Therefore, these new therapeutic modalities may particularly benefit undeserved populations with aggressive cancers. CBD is a novel compound by which the growth and spread of breast cancer may potentially be inhibited through down-regulation of Id-1. We have outlined a strategy to create a family of breast cancer inhibitors that are even more active than the parent drug CBD. Additionally, we expect to discover the detailed mechanisms involved in cannabinoid inhibition of Id-1 and corresponding breast cancer cell aggressiveness. We are collaborating with a pharmaceutical company who is currently engaged in clinical trials testing the efficacy of CBD for indications unrelated to cancer. If CBD inhibits Id-1 and corresponding breast cancer metastasis in mouse models, there would be significant enthusiasm to move CBD toward clinical trials for the treatment of metastatic breast cancer. This process could be rapid since CBD is already being tested in the clinic for indication other then cancer and has an established safety profile. Our goal is to start clinical trials with CBD within three years. Our long-term goal is to follow up with second generation CBD analogs that are expected to be more potent and/or efficacious at inhibiting metastatic breast cancer in humans compared to CBD.
Article Source: http://www.examiner.com/
Image: Northern California Bud. Photo by Adrian Miles
And to think that cannabidiol, a non-psycotropic chemical that can stop cancer metastasis, is a Schedule 1 drug in the USA.
Wait a year or two and there will be a synthesized chemical copy of cannabidiol made in a lab. That will be legal, the pharma company with the patent probably won’t use it however because, if it can stop the spreading of the cancer, less (money making) cancer drugs will be needed. Thank guys, great work! /sarcasm
Also as I understand it, CBD usually accompanies THC in approx 4:6 ratio and is responsible for regulating the high caused by THC (as it affects how the THC is absorbed by the cannabinoid receptor). This ratio can vary from strain to strain however. Now my assumption is that without the CBD, strange shit can happen, which is why people taking marinol (lab-made THC) can skitz out. I also assume that the Skunk weed available in the UK is a strain bred with a low CBD to THC ratio, making the users of that strain skitz out as well.
Am I correct in my assumptions? Can anyone refute this?
Great submit! Extremely full and also depth details. That�s just what i would like! Done well!