Raup-Konsavage Wesley M, Johnson Megan, Legare Christopher A, Yochum Gregory S, Morgan Daniel J, Vrana Kent E
Department of Pharmacology, Pennsylvania State University College of Medicine, Hershey, Pennsylvania.
Department of Biochemistry and Molecular Biology, Pennsylvania State University College of Medicine, Hershey, Pennsylvania.
Cannabis Cannabinoid Res. 2018 Dec 21;3(1):272-281. doi: 10.1089/can.2018.0065. eCollection 2018.
Colorectal cancer (CRC) is a leading cause of cancer-related deaths worldwide, and new therapeutic strategies are still required. Here we screened a synthetic cannabinoid library to identify compounds that uniformly reduce the viability of seven CRC cell lines. Seven distinct CRC cell lines were treated with 10 μM cannabinoid compounds (from a library of 370 molecules) for 48 h, and cell viability was subsequently measured with MTS assay. Dose-response curves were conducted for compounds that were found to reproducibly reduce cell viability of one or more cell lines. We identified 10 compounds from the library that were able to reduce cell viability of CRC cell lines (with an IC ≤ 30 μM). Of these compounds, seven were specific for CRC cells, and six were effective in all CRC cell lines tested. Treatment with traditional phytocannabinoids (THC or CBD) was either ineffective or much less potent and only partially efficacious. Treatment with antagonists for the known cannabinoid receptors (alone or in combination) failed to block the activity of the most potent of identified compounds. We identified three families of cannabinoid compounds that reduce CRC cell viability through a noncanonical receptor mechanism. Future modification of these compounds may lead to the development of novel therapies to treat this disease.
结直肠癌(CRC)是全球癌症相关死亡的主要原因之一,仍然需要新的治疗策略。在此,我们筛选了一个合成大麻素文库,以鉴定能一致降低七种结直肠癌细胞系活力的化合物。用10μM大麻素化合物(来自一个包含370个分子的文库)处理七种不同的结直肠癌细胞系48小时,随后用MTS法测量细胞活力。对那些被发现能可重复降低一种或多种细胞系细胞活力的化合物进行剂量反应曲线测定。我们从文库中鉴定出10种能够降低结直肠癌细胞系细胞活力的化合物(IC≤30μM)。在这些化合物中,七种对结直肠癌细胞具有特异性,六种对所有测试的结直肠癌细胞系均有效。用传统植物大麻素(THC或CBD)处理要么无效,要么效力低得多且仅部分有效。用已知大麻素受体拮抗剂单独或联合处理未能阻断所鉴定的最有效化合物的活性。我们鉴定出三类通过非经典受体机制降低结直肠癌细胞活力的大麻素化合物。对这些化合物的进一步修饰可能会导致开发出治疗这种疾病的新疗法。