PJ34 hydrochloride is an effective and specific PARP inhibitor with an IC50 value of 110nM [1]. PJ34 hydrochloride promotes cell death by inhibiting PARP1-mediated DNA repair, and leads to a decrease in NF-κB expression and specifically blocks the mitosis of cancer cells[2]. PJ34 hydrochloride has been widely used to kill tumor cells and has been employed in the development of novel combined therapies to efficiently enhance the cytotoxicity of chemotherapy drugs[3].
In vitro, PJ34 hydrochloride treatment for 48 hours significantly inhibited the viability of OVCAR-3 cells and SKOV-3 cells, with the IC50 values being 18.7µM and 28.5µM, respectively[4]. Treatment with 50µM PJ34 hydrochloride for 72 hours induced cell cycle arrest and apoptosis in HTLV-I-transformed MT-2 cells[5]. Treatment with 10µM PJ34 hydrochloride for 24 hours resulted in mitotic defects in M14 cells and promoted abnormal accumulation of actin in the nucleolus[6].
In vivo, PJ34 hydrochloride treatment via intraperitoneal injection at a dose of 10mg/kg three times weekly for 4 weeks alleviated the accumulation of triglycerides (TG) in the liver of alcohol-fed mice and reduced the hepatic gene expression of sterol regulatory element-binding protein 1c, DGAT1, and DGAT2[7]. Intraperitoneal injection of PJ34 hydrochloride (50μg) at 2 hours before and 6 hours after middle cerebral artery occlusion (MCAo) significantly reduced the cerebral infarct volume in SV/129 mice [8].
References:
[1] Iwashita A, Tojo N, Matsuura S, et al. A novel and potent poly (ADP-ribose) polymerase-1 inhibitor, FR247304 (5-chloro-2-[3-(4-phenyl-3, 6-dihydro-1 (2 H)-pyridinyl) propyl]-4 (3 H)-quinazolinone), attenuates neuronal damage in in vitro and in vivo models of cerebral ischemia[J]. The Journal of pharmacology and experimental therapeutics, 2004, 310(2): 425-436.
[2] Cohen-Armon M. The modified phenanthridine PJ34 unveils an exclusive cell-death mechanism in human cancer cells[J]. Cancers, 2020, 12(6): 1628.
[3] Mann M, Chauhan S S, Kumar S, et al. PJ34-mediated PARP-1 enzymatic activity inhibition in cervical cancer modulates the cellular response to cisplatin[J]. Cancer Research, 2016, 76(14_Supplement): 2152-2152.
[4] Güler A E, Tuncer M C, Özdemir İ. Synergistic Antitumor Activity of Curcumin and the PARP1 Inhibitor PJ34 in Platinum-Sensitive and Resistant Ovarian Cancer Cells[J]. Cancers, 2026, 18(4): 620.
[5] Bai X T, Moles R, Chaib-Mezrag H, et al. Small PARP inhibitor PJ-34 induces cell cycle arrest and apoptosis of adult T-cell leukemia cells[J]. Journal of hematology & oncology, 2015, 8(1): 117.
[6] Chevanne M, Zampieri M, Caldini R, et al. Inhibition of PARP activity by PJ‐34 leads to growth impairment and cell death associated with aberrant mitotic pattern and nucleolar actin accumulation in M14 melanoma cell line[J]. Journal of cellular physiology, 2010, 222(2): 401-410.
[7] Huang S, Zhang B, Chen Y, et al. Poly (ADP-ribose) polymerase inhibitor PJ34 attenuated hepatic triglyceride accumulation in alcoholic fatty liver disease in mice[J]. The Journal of pharmacology and experimental therapeutics, 2018, 364(3): 452-461.
[8] Abdelkarim G E, Gertz K, Harms C, et al. Protective effects of PJ34, a novel, potent inhibitor of poly (ADP-ribose) polymerase (PARP) in in vitro and in vivo models of stroke[J]. International journal of molecular medicine, 2001, 7(3): 255-260.