Researchers at the University of East Anglia in UK and colleagues have discovered previously unknown signalling platforms which are responsible for the drug's success in shrinking tumours.
It is hoped that the research co-led with the Universidad Complutense de Madrid, Spain could help develop a synthetic equivalent with anti-cancer properties.
The team used samples of human cancer cells to induce tumours in mice. They then targeted the tumours with doses of the cannabis compound THC (Tetrahydrocannabinol).
They found that two cell receptors in particular were responsible for the drug's anti-tumour effects.
"However, it was unclear which of these receptors were responsible for the anti-tumour effects of THC.
"We show that these effects are mediated via the joint interaction of CB2 and GPR55 - two members of the cannabinoid receptor family.
"Our findings help explain some of the well-known but still poorly understood effects of THC at low and high doses on tumour growth," he said.
McCormick added that cancer sufferers should not be tempted to self-medicate.
The research is published in the Journal of Biological Chemistry.
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