|Table of Contents|

The anticancer effects and mechanism of Irisin and Irisin-liposomes in non-small cell lung cancer

Journal Of Modern Oncology[ISSN:1672-4992/CN:61-1415/R]

Issue:
2024 10
Page:
1792-1798
Research Field:
Publishing date:

Info

Title:
The anticancer effects and mechanism of Irisin and Irisin-liposomes in non-small cell lung cancer
Author(s):
YU Zhihui1YUAN Bin2ZHUGE Xiangzhen3YU Xiangyuan4
1.Department of Respiratory and Critical Care Medicine,Nanxishan Hospital of Guangxi Zhuang Autonomous Region,Guangxi Guilin 541000,China;2.Department of Respiratory and Critical Care Medicine,Miluo People's Hospital,Hunan Miluo 414400,China;3.Department of Clinical Nutrition,Affiliated Hospital of Guilin Medical University,Guangxi Guilin 541000,China;4.School of Public Health,Guilin Medical University,Guangxi Guilin 541000,China.
Keywords:
Irisinliposomesnon-small cell lung cancerferroptosisROS
PACS:
R734.2
DOI:
10.3969/j.issn.1672-4992.2024.10.005
Abstract:
Objective:To investigate the effects of Irisin and Irisin-liposomes (LPs) on human non-small cell lung cancer H1299 cells and their potential mechanisms of action.Methods:Nanoparticle characterization and cellular mitochondrial morphology were observed by transmission electron microscopy.CCK8 and flow cytometry were used to analyze the effects of Irisin and Irisin-LPs on cell viability,apoptosis,and cycling of H1299 cells.qRT-PCR and Western blot were used to analyze the effects of Irisin on Nrf2/HO-1 signaling.Results:Irisin and Irisin-LPs significantly inhibited the growth and cell cycle of H1299 cells and promoted their apoptosis,with Irisin-LPs having a more pronounced effect.Irisin and Irisin-LPs significantly altered cytoskeletal structures and mitochondrial functions as revealed by cytoskeleton staining and mitochondrial membrane potential detection.Furthermore,Irisin and Irisin-LPs significantly induced iron-dependent lipid peroxidation,i.e.,ferroptosis.In addition,Irisin and Irisin-LPs significantly regulated the expression of the Nrf2/HO-1 signaling pathway.Conclusion:This study reveals the anti-lung cancer activity and potential mechanisms of Irisin and Irisin-LPs,providing new theoretical and experimental evidence for the clinical application of Irisin.

References:

[1] CHEN P,LIU Y,WEN Y,et al.Non-small cell lung cancer in China [J].Cancer Commun (Lond),2022,42(10):937-970.
[2] BASSE C,SWALDUZ A,LEER A,et al.NSCLC and new oncogenic mutations:Diagnosis and perspectives[J].Rev Mal Respir,2021,38(5):477-488.
[3] CASTRO G,KUDABA I,WU YL,et al.Five-year outcomes with pembrolizumab versus chemotherapy as first-line therapy in patients with non-small-cell lung cancer and programmed death ligand-1 tumor proportion score >/= 1% in the KEYNOTE-042 study [J].J Clin Oncol,2023,41(11):1986-1991.
[4] LIU S,CUI F,NING K,et al.Role of irisin in physiology and pathology [J].Front Endocrinol (Lausanne),2022,13:962968.
[5] KAM TI,PARK H,CHOU SC,et al.Amelioration of pathologic alpha-synuclein-induced Parkinson's disease by irisin [J].Proc Natl Acad Sci USA,2022,119(36):e2204835119.
[6] WOZNIAK S,NOWINSKA K,CHABOWSKI M,et al.Significance of Irisin (FNDC5) expression in colorectal cancer [J].In Vivo,2022,36(1):180-188.
[7] LIU J,SONG N,HUANG Y,et al.Irisin inhibits pancreatic cancer cell growth via the AMPK-mTOR pathway [J].Sci Rep,2018,8(1):15247.
[8] ZHANG ZP,ZHANG XF,LI H,et al.Serum irisin associates with breast cancer to spinal metastasis [J].Medicine (Baltimore),2018,97(17):e0524.
[9] NOWINSKA K,JABLONSKA K,PAWELCZYK K,et al.Expression of Irisin/FNDC5 in cancer cells and stromal fibroblasts of non-small cell lung cancer [J].Cancers (Basel),2019,11(10):1538.
[10] GUIMARAES D,CAVACO-PAULO A,NOGUEIRA E.Design of liposomes as drug delivery system for therapeutic applications [J].Int J Pharm,2021,601:120571.
[11] FAN Y,MARIOLI M,ZHANG K.Analytical characterization of liposomes and other lipid nanoparticles for drug delivery [J].J Pharm Biomed Anal,2021,192:113642.
[12] SHAO L,LI H,CHEN J,et al.Irisin suppresses the migration,proliferation,and invasion of lung cancer cells via inhibition of epithelial-to-mesenchymal transition [J].Biochem Biophys Res Commun,2017,485(3):598-605.
[13] JIANG X,STOCKWELL BR,CONRAD M.Ferroptosis:mechanisms,biology and role in disease [J].Nat Rev Mol Cell Biol,2021,22(4):266-282.
[14] TA N,QU C,WU H,et al.Mitochondrial outer membrane protein FUNDC2 promotes ferroptosis and contributes to doxorubicin-induced cardiomyopathy [J].Proc Natl Acad Sci USA,2022,119(36):e2117396119.
[15] WEI S,QIU T,YAO X,et al.Arsenic induces pancreatic dysfunction and ferroptosis via mitochondrial ROS-autophagy-lysosomal pathway [J].J Hazard Mater,2020,384:121390.
[16] YANG W,WANG Y,ZHANG C,et al.Maresin1 protect against ferroptosis-induced liver injury through ROS inhibition and Nrf2/HO-1/GPX4 activation [J].Front Pharmacol,2022,13:865689.
[17] HAN S,LIN F,QI Y,et al.HO-1 contributes to luteolin-triggered ferroptosis in clear cell renal cell carcinoma via increasing the labile iron pool and promoting lipid peroxidation [J].Oxid Med Cell Longev,2022,2022:3846217.
[18] DOHOPOLSKI M,GOTTUMUKKALA S,GOMEZ D,et al.Radiation therapy in non-small-cell lung cancer [J].Cold Spring Harb Perspect Med,2021,11(10):a037713.
[19] 封小红,陶冀.晚期非小细胞肺癌免疫治疗与消融治疗的研究进展[J].现代肿瘤医学,2021,29(20):3684-3689. FENG XH,TAO J.Advances in immunotherapy and ablative therapy for advanced NSCLC[J].Modern Oncology,2021,29(20):3684-3689.
[20] YU X,LI Y,JIANG G,et al.FGF21 promotes non-small cell lung cancer progression by SIRT1/PI3K/AKT signaling [J].Life Sci,2021,269:118875.
[21] WANG X,LU Y,QIN Z,et al.Stereotactic body radiotherapy and conventional radiotherapy induce cytoskeleton extension and enlargement of cell morphology in non-small cell lung cancer [J].Dose Response,2021,19(4):15593258211064499.
[22] PRABHU KS,BHAT AA,SIVEEN KS,et al.Sanguinarine mediated apoptosis in non-small cell lung cancer via generation of reactive oxygen species and suppression of JAK/STAT pathway [J].Biomed Pharmacother,2021,144:112358.
[23] MA CJ,ZHANG W,ZENG J,et al.Progress in the study of mechanisms regulating ferroptosis [J].Journal of Biology,2021,38(4):109-113.
[24] GAN B.Mitochondrial regulation of ferroptosis [J].J Cell Biol,2021,220(9):e202105043.
[25] SHEN C,WANG Y.Ferroptosis biomarkers for predicting prognosis and immunotherapy efficacy in adrenocortical carcinoma [J].Arch Med Res,2023,54(1):45-55.
[26] LI D,WANG Y,DONG C,et al.CST1 inhibits ferroptosis and promotes gastric cancer metastasis by regulating GPX4 protein stability via OTUB1[J].Oncogene,2023,42(2):83-98.
[27] WANG J,ZHU Q,WANG Y,et al.Irisin protects against sepsis-associated encephalopathy by suppressing ferroptosis via activation of the Nrf2/GPX4 signal axis [J].Free Radic Biol Med,2022,187:171-184.
[28] LIU L,KANG XX.ACSL4 is overexpressed in psoriasis and enhances inflammatory responses by activating ferroptosis [J].Biochem Biophys Res Commun,2022,623:1-8.
[29] ZHAO Y,CAI J,SHI K,et al.Germacrone induces lung cancer cell apoptosis and cell cycle arrest via the Akt/MDM2/p53 signaling pathway [J].Mol Med Rep,2021,23(6):452.
[30] 彭彩霞,王晓峰,王聪.p53抑癌基因在腺样囊性癌中的作用[J].现代肿瘤医学,2016,24(6):1014-1016. PENG CX,WANG XF,WANG C.Progress of p53 tumor suppressor gene in adenoid cystic carcinoma[J].Modern Oncology,2016,24(6):1014-1016.
[31] DUAN C,WANG H,JIAO D,et al.Curcumin restrains oxidative stress of after intracerebral hemorrhage in rat by activating the Nrf2/HO-1 pathway [J].Front Pharmacol,2022,13:889226.

Memo

Memo:
广西医疗卫生重点学科建设项目
Last Update: 1900-01-01