Chemical composition and pharmacological bio-efficacy of Parrotiopsis jacquemontiana (Decne) Rehder for anticancer activity

被引:8
|
作者
Ali, Saima [1 ]
Khan, Muhammad Rashid [1 ]
Iqbal, Javed [2 ]
Batool, Riffat [1 ]
Naz, Irum [1 ]
Yaseen, Tabassum [2 ]
Abbasi, Banzeer Ahsan [3 ]
Nasir, Jamal Abdul [4 ]
El-Serehy, Hamed A. [5 ]
机构
[1] Quaid I Azam Univ, Fac Biol Sci, Dept Biochem, Islamabad 45320, Pakistan
[2] Bacha Khan Univ, Dept Bot, Charsadda, Khyber Pakhtunk, Pakistan
[3] Quaid I Azam Univ, Dept Plant Sci, Islamabad 45320, Pakistan
[4] UCL, Dept Chem, Kathleen Lonsdale Mat Chem, 20 Gordon St, London WC1H 0AJ, England
[5] King Saud Univ, Coll Sci, Dept Zool, Riyadh 11451, Saudi Arabia
关键词
Parrotiopsis jacquemontiana; Cancer; Apoptosis; STAT3; HCCLM3; MDA-MB; 231; Stattic; STAT3 SIGNALING PATHWAY; ESSENTIAL OIL; IN-VITRO; HEPATOCELLULAR-CARCINOMA; ANTIMICROBIAL ACTIVITY; CURRENT LANDSCAPE; URSOLIC ACID; TUMOR-GROWTH; APOPTOSIS; BREAST;
D O I
10.1016/j.sjbs.2021.07.072
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Consistent STAT3 (Single transducer and activator of transcription 3) activation is observed in many tumors and promotes malignant cell transformation. In the present investigation, we evaluated the anti-cancer effects of Parrotiopsis jacquemontiana methanol fraction (PJM) on STAT3 inhibition in HCCLM3 and MDA-MB 231 cells. PJM suppressed the activation of upstream kinases i.e. JAK-1/2 (Janus kinase-1/2), and c-Src (Proto-oncogene tyrosine-protein kinase c-Src), and upregulated the expression levels of PIAS-1/3 (Protein Inhibitor of Activated STATs-1/3), SHP-1/2 (Src-homology region 2 domain-containing phosphatase-1/2), and PTP-1B (Protein tyrosine phosphatase 1 B) which negatively regulate STAT3 signal -ing pathway. PJM also decreased the levels of protein products conferring to various oncogenes, which in turn repressed the proliferation, migration, invasion, and induced apoptosis in cancer cell lines. The growth inhibitory effects of PJM on cell-cycle and metastasis were correlated with decreased expression levels of CyclinD1, CyclinE, MMP-2 (Matrix metalloproteinases-2), and MMP-9 (Matrix metalloproteinases-9). Induction of apoptosis was indicated by the cleavage and subsequent activation of Caspases (Cysteine-dependent Aspartate-directed Proteases) i.e. caspase-3, 7, 8, 9, and PARP (Poly (ADP-ribose) polymerase) as well as through the down-regulation of anti-apoptotic proteins. These apop-totic effects of PJM were preceded by inhibition of STAT3 cell-signaling pathway. STAT3 was needed for PJM-induced apoptosis, and inhibition of STAT3 via pharmacological inhibitor (Stattic; SC-203282) abol-ished the apoptotic effects. Conclusively, our results demonstrate the capability of PJM to inhibit cancer cell-proliferation and induce apoptosis by suppressing STAT3 via upregulation of STAT3 inhibitors and pro-apoptotic proteins whereas the down-regulation of upstream kinases and anti-apoptotic protein expression. In future, one-step advance studies of PHM regarding its role in metastatic inhibition, immune response modulation for reducing tumor, and inducing apoptosis in suitable animal models would be an interesting and promising research area. (c) 2021 The Author(s). Published by Elsevier B.V. on behalf of King Saud University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:4969 / 4986
页数:18
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