Bienvenue-Pariseault Josianne, Sagrillo-Fagundes Lucas, Wong-Yen Philippe, Stakamatos Darius, Cohen Marie, Vaillancourt Cathy
Institut national de la recherche scientifique (INRS) - Centre Armand-Frappier Santé Biotechnologie (AFSB), Laval, Canada.
CIUSSS-Nord-de-l'île-de-Montréal, Montreal, Canada.
J Pineal Res. 2025 Sep;77(5):e70072. doi: 10.1111/jpi.70072.
Melatonin, an indolamine primarily recognized for regulating circadian rhythms, has also demonstrated notable antitumoral properties. Melatonin induces endoplasmic reticulum (ER) stress, modulates autophagy, and promotes apoptosis in various tumors, including gastric, ovarian, cervical, oral tongue, colorectal, renal, hepatic, and bladder cancer. In placental choriocarcinoma, melatonin reduces cell viability and induces apoptosis by inhibiting autophagy and disrupting the mitochondrial membrane potential. However, its effects on ER stress and the unfolded protein response (UPR) pathway remain unexplored. It is hypothesized here that the proapoptotic effects of melatonin in choriocarcinoma cells occur through the activation of the UPR pathway. The factors implicated in the UPR (PERK, IRE1ɑ, ATF6, GRP78, ATF4, CHOP, P-eIF2α) pathways were evaluated by Western blot, RT-qPCR, and flow cytometry in BeWo (human choriocarcinoma) cells treated with or without melatonin (1 mM). Melatonin significantly increased protein levels of GRP78 (p = 0.0329), IRE1α (p = 0.0394), p-eIF2α (p = 0.0439), ATF4 (p = 0.0267), CHOP (p = 0.0379), Bax and cleaved PARP but did not affect TRAF2 and NFkB protein levels nor XBP1 mRNA splicing. PERK knockdown, via siRNA, prevented the rise in GRP78, p-eIF2α/eIF2α, and ATF4 levels by melatonin. Additionally, melatonin increased early apoptosis in BeWo cells (p = 0.0371) and PERK knockdown increased the susceptibility of BeWo cells to apoptosis when treated with tunicamycin (p = 0.0359), suggesting that ER stress plays a role in BeWo cell survival. This study demonstrates that melatonin activates the PERK-ATF4-P-eIF2α-CHOP pathway and induces early apoptosis in BeWo cells, while PERK deficiency compromises cell survival under ER stress. Our findings suggest that modulating PERK-UPR signaling with melatonin could present a promising therapeutic strategy for cancer, including placental choriocarcinoma.
褪黑素是一种主要因调节昼夜节律而为人所知的吲哚胺,它也表现出显著的抗肿瘤特性。褪黑素可诱导内质网(ER)应激、调节自噬,并在包括胃癌、卵巢癌、宫颈癌、口腔舌癌、结直肠癌、肾癌、肝癌和膀胱癌在内的多种肿瘤中促进细胞凋亡。在胎盘绒毛膜癌中,褪黑素通过抑制自噬和破坏线粒体膜电位来降低细胞活力并诱导细胞凋亡。然而,其对内质网应激和未折叠蛋白反应(UPR)途径的影响仍未得到探索。本文假设褪黑素在绒毛膜癌细胞中的促凋亡作用是通过激活UPR途径实现的。通过蛋白质免疫印迹法、逆转录定量聚合酶链反应(RT-qPCR)和流式细胞术,对用或不用褪黑素(1 mM)处理的BeWo(人绒毛膜癌)细胞中UPR(蛋白激酶RNA样内质网激酶(PERK)、肌醇需求酶1α(IRE1ɑ)、活化转录因子6(ATF6)、葡萄糖调节蛋白78(GRP78)、ATF4、C/EBP同源蛋白(CHOP)、磷酸化真核翻译起始因子2α(P-eIF2α))途径中的相关因子进行了评估。褪黑素显著提高了GRP78(p = 0.0329)、IRE1α(p = 0.0394)、P-eIF2α(p = 0.0439)、ATF4(p = 0.0267)、CHOP(p = 0.0379)、Bax和裂解的聚(ADP-核糖)聚合酶(PARP)的蛋白水平,但不影响肿瘤坏死因子受体相关因子2(TRAF2)和核因子κB(NFkB)的蛋白水平,也不影响XBP1 mRNA的剪接。通过小干扰RNA(siRNA)敲低PERK可阻止褪黑素引起的GRP78、P-eIF2α/eIF2α和ATF4水平升高。此外,褪黑素增加了BeWo细胞中的早期凋亡(p = 0.0371),而敲低PERK增加了BeWo细胞在用衣霉素处理时对凋亡的敏感性(p = 0.0359),这表明内质网应激在BeWo细胞存活中起作用。本研究表明,褪黑素激活PERK-ATF4-P-eIF2α-CHOP途径并诱导BeWo细胞早期凋亡,而PERK缺乏会损害内质网应激条件下的细胞存活。我们的研究结果表明,用褪黑素调节PERK-UPR信号可能为包括胎盘绒毛膜癌在内的癌症提供一种有前景的治疗策略。