Abstract

Cannabinoids (CBs) from Cannabis sativa provide relief for tumor-associated symptoms (including nausea, anorexia, and neuropathic pain) in the palliative treatment of cancer patients. Additionally, they may decelerate tumor progression in breast cancer patients. Indeed, the psychoactive delta-9-tetrahydrocannabinol (THC), non-psychoactive cannabidiol (CBD) and other CBs inhibited disease progression in breast cancer models. The effects of CBs on signaling pathways in cancer cells are conferred via G-protein coupled CB-receptors (CB-Rs), CB1-R and CB2-R, but also via other receptors, and in a receptor-independent way. THC is a partial agonist for CB1-R and CB2-R; CBD is an inverse agonist for both. In breast cancer, CB1-R expression is moderate, but CB2-R expression is high, which is related to tumor aggressiveness. CBs block cell cycle progression and cell growth and induce cancer cell apoptosis by inhibiting constitutive active pro-oncogenic signaling pathways, such as the extracellular-signal-regulated kinase pathway. They reduce angiogenesis and tumor metastasis in animal breast cancer models. CBs are not only active against estrogen receptor-positive, but also against estrogen-resistant breast cancer cells. In human epidermal growth factor receptor 2-positive and triple-negative breast cancer cells, blocking protein kinase B- and cyclooxygenase-2 signaling via CB2-R prevents tumor progression and metastasis. Furthermore, selective estrogen receptor modulators (SERMs), including tamoxifen, bind to CB-Rs; this process may contribute to the growth inhibitory effect of SERMs in cancer cells lacking the estrogen receptor. In summary, CBs are already administered to breast cancer patients at advanced stages of the disease, but they might also be effective at earlier stages to decelerate tumor progression.

Highlights

  • Cannabis sativa and CannabinoidsCannabis sativa (C. sativa) was known among ancient Asian, African, and European agricultural societies

  • In human epidermal growth factor receptor 2-positive and triple-negative breast cancer cells, blocking protein kinase B- and cyclooxygenase-2 signaling via CB2-R prevents tumor progression and metastasis

  • Many constituents of C. sativa, such as CBD and THC, exhibit beneficial anti-inflammatory or antitumoral properties. They act through the CB-Rs, CB1-R, and CB2-R

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Summary

Introduction

Cannabis sativa (C. sativa) was known among ancient Asian, African, and European agricultural societies. Application of C. sativa in industry and medicine is experiencing a revival. The C. sativa plant contains >500 as a source of compounds to treat cancer and life-threating diseases. A high THC/CBD ratio is responsible for the euphoric, relaxing, andofanxiolytic of medical cannabis (marijuana), whereas, a highratio. Cultivation from different varieties of C. sativa produces two main varieties with distinct concentrations of CBs, and the discrimination from the THC/CBD ratio divides commercial cannabis. Cultivation from different varieties of C. sativa produces two main varieties with distinct concentrations of CBs, and the discrimination from the THC/CBD ratio divides commercial cannabis strains into three principal chemotypes. Industrial C. sativa flowers (chemotype II and III flowers) contain less than 0.3% THC and CBD levels are 10–12% when calculated for dry weight [6]. CBs with different properties that can block or activate CB-receptors (CB-Rs) may be useful in cancer treatment [7,8]

Mechanism of Cannabinoid Action
Mechanism ofbreast
Cannabinoids from Cannabis sativa
Minor Phytocannabinoids
Synthetic Cannabinoid Analogues
Molecular Effects of CBs in Breast Cancer
Cannabinoid Receptor Signaling
Phytocannabinoids and Synthetic Analogues
Endocannabinoids
Preclinical Evidence of the Effects of CBs in Animal Models
Effect of Cannabinoids Related to Estrogen
Current
Findings
Summary
Full Text
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