|Table of Contents|

Research status of neutral sphingomyelinase-2 in the occurrence and development of cancer

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

Issue:
2022 04
Page:
713-717
Research Field:
Publishing date:

Info

Title:
Research status of neutral sphingomyelinase-2 in the occurrence and development of cancer
Author(s):
WANG HongxuWEI ShihuiMI ShichaoSUN LiYUAN Shengtao
New Drug Screening Center,China Pharmaceutical University,Jiangsu Nanjing 210009,China.
Keywords:
nSMase2cancerapoptosisexosomes
PACS:
R730
DOI:
10.3969/j.issn.1672-4992.2022.04.033
Abstract:
Sphingomyelin-ceramide metabolism is related to various cellular processes such as oxidative stress,cell proliferation and cell necrosis,and is involved in some physiological and pathological processes such as aging,obesity and diabetes.Neutral sphingomyelinase-2 (nSMase2),a key enzyme in the metabolic pathway of sphingomyelin,can hydrolyze sphingomyelin to produce ceramide and phosphocholine,involved in cell apoptosis,proliferation,inflammation and many other biological functions.In recent years,many studies have shown that nSMase2 affects the progression of certain tumors.This article mainly reviews the enzymatic role of nSMase2,the relationship between nSMase2 and cancers and the effects of nSMase2 in tumor cell apoptosis,proliferation,and exosomes secretion,in order to fully understand the function of nSMase2 in cancer.

References:

[1] JEFFRIES KA,KRUPENKO NI.Ceramide signaling and p53 pathways[J].Adv Cancer Res,2018,140:191-215.
[2] INSAUSTI-URKIA N,SOLSONA-VILARRASA E,GARCIA-RUIZ C,et al.Sphingomyelinases and liver diseases[J].Biomolecules,2020,10(11):1497.
[3] PARSIEGLA G,NOGUERE C,SANTELL L,et al.The structure of human DNase I bound to magnesium and phosphate ions points to a catalytic mechanism common to members of the DNase I-like superfamily[J].Biochemistry,2012,51(51):10250-10258.
[4] HOFMANN K,TOMIUK S,WOLFF G,et al.Cloning and characterization of the mammalian brain-specific,Mg2+-dependent neutral sphingomyelinase[J].Proc Natl Acad Sci USA,2000,97(11):5895-5900.
[5] WU BX,CLARKE CJ,MATMATI N,et al.Identification of novel anionic phospholipid binding domains in neutral sphingomyelinase 2 with selective binding preference[J].J Biol Chem,2011,286(25):22362-22371.
[6] AIROLA MV,SHANBHOGUE P,SHAMSEDDINE AA,et al.Structure of human nSMase2 reveals an interdomain allosteric activation mechanism for ceramide generation[J].Proc Natl Acad Sci USA,2017,114(28):E5549-E5558.
[7] NGANGA R,OLEINIK N,OGRETMEN B.Mechanisms of ceramide-dependent cancer cell death[J].Adv Cancer Res,2018,140:1-25.
[8] OGRETMEN B.Sphingolipid metabolism in cancer signalling and therapy[J].Nat Rev Cancer,2018,18(1):33-50.
[9] HERNANDEZ-TIEDRA S,FABRIAS G,DAVILA D,et al.Dihydroceramide accumulation mediates cytotoxic autophagy of cancer cells via autolysosome destabilization[J].Autophagy,2016,12(11):2213-2229.
[10] KITATANI K,USUI T,SRIRAMANSK,et al.Ceramide limits phosphatidylinositol-3-kinase C2β-controlled cell motility in ovarian cancer:potential of ceramide as a metastasis-suppressor lipid[J].Oncogene,2016,35(21):2801-2812.
[11] WANG P,YUAN Y,LIN W,et al.Roles of sphingosine-1-phosphate signaling in cancer[J].Cancer Cell Int,2019,19:295.
[12] UEDA N.Ceramide-induced apoptosis in renal tubular cells:a role of mitochondria and sphingosine-1-phoshate[J].Int J Mol Sci,2015,16(3):5076-5124.
[13] ZHONG L,KONG JN,DINKINS MB,et al.Increased liver tumor formation in neutral sphingomyelinase-2-deficient mice[J].J Lipid Res,2018,59(5):795-804.
[14] WANG J,LI J,GU J,et al.Abnormal methylation status of FBXW10 and SMPD3,and associations with clinical characteristics in clear cell renal cell carcinoma[J].Oncol Lett,2015,10(5):3073-3080.
[15] KIM WJ,OKIMOTO RA,PURTON LE,et al.Mutations in the neutral sphingomyelinase gene SMPD3 implicate the ceramide pathway in human leukemias[J].Blood,2008,111(9):4716-4722.
[16] MIRANDA I.Overexpression of nSMase2 in 4T1 and E0771 breast cancer cells confers varying oncogenic properties[D].Stony Brook:State University of New York,2019:1-43.
[17] LIU M,ZHU K,QIAN X,et al.Identification of miRNA/mRNA-negative regulation pairs in nasopharyngeal carcinoma[J].Med Sci Monit,2016,22:2215-2234.
[18] SHAKOR AB,ATIA M,ISMAIL IA,et al.Curcumin induces apoptosis of multidrug-resistant human leukemia HL60 cells by complex pathways leading to ceramide accumulation[J].Biochim Biophys Acta,2014,1841(12):1672-1682.
[19] CHIPUK JE,MCSTAY GP,BHARTI A,et al.Sphingolipid metabolism cooperates with BAK and BAX to promote the mitochondrial pathway of apoptosis[J].Cell,2012,148(5):988-1000.
[20] SHAMSEDDINE AA,CLARKE CJ,CARROLL B,et al.p53-dependent upregulation of neutral sphingomyelinase-2:role in doxorubicin-induced growth arrest[J].Cell Death Dis,2015,6(10):e1947.
[21] LUBERTO C,HASSLER DF,SIGNORELLI P,et al.Inhibition of tumor necrosis factor-induced cell death in MCF7 by a novel inhibitor of neutral sphingomyelinase[J].J Biol Chem,2002,277(43):41128-41139.
[22] SHAKOR AB,ATIA M,ISMAIL IA,et al.Curcumin induces apoptosis of multidrug-resistant human leukemia HL60 cells by complex pathways leading to ceramide accumulation[J].Biochim Biophys Acta,2014,1841(12):1672-1682.
[23] MONDAL S,MANDAL C,SANGWAN R,et al.Withanolide D induces apoptosis in leukemia by targeting the activation of neutral sphingomyelinase-ceramide cascade mediated by synergistic activation of c-Jun N-terminal kinase and p38 mitogen-activated protein kinase[J].Mol Cancer,2010,9(1):1-17.
[24] MARCHESINI N,OSTA W,BIELAWSKI J,et al.Role for mammalian neutral sphingomyelinase 2 in confluence-induced growth arrest of MCF7 cells[J].J Biol Chem,2004,279(24):25101-25111.
[25] BESIM OGRETMEN,JACQUELINE M KRAVEKA,DEBORAH SCHADY,et al.Molecular mechanisms of ceramide-mediated telomerase inhibition in the A549 human lung adenocarcinoma cell line[J].J Biol Chem,2001,276(35):32506-32514.
[26] CODINI M,CONTE C,CATALDI S,et al.Nuclear lipid microdomains regulate daunorubicin resistance in hepatoma cells[J].Int J Mol Sci,2018,19(11):3424.
[27] CLARKE CJ,SHAMSEDDINE AA,JACOB JJ,et al.ATRA transcriptionally induces nSMase2 through CBP/p300-mediated histone acetylation[J].J Lipid Res,2016,57(5):868-881.
[28] AHEGET H,MAZINI L,MARTIN F,et al.Exosomes:their role in pathogenesis,diagnosis and treatment of diseases[J].Cancers (Basel),2020,13(1):84.
[29] KOSAKA N,IGUCHI H,HAGIWARA K,et al.Neutral sphingomyelinase 2 (nSMase2)-dependent exosomal transfer of angiogenic microRNAs regulate cancer cell metastasis[J].J Biol Chem,2013,288(15):10849-10859.
[30] SINGH R,POCHAMPALLY R,WATABE K,et al.Exosome-mediated transfer of miR-10b promotes cell invasion in breast cancer[J].Molecular Cancer,2014,13(1):1-11.
[31] KONG JN,HE Q,WANG G,et al.Guggulsterone and bexarotene induce secretion of exosome-associated breast cancer resistance protein and reduce doxorubicin resistance in MDA-MB-231 cells[J].Int J Cancer,2015,137(7):1610-1620.
[32] BASTOS N,RUIVO CF,DA SILVA S,et al.Exosomes in cancer:Use them or target them[J].Semin Cell Dev Biol,2018,78:13-21.
[33] KUBOTA S,CHIBA M,WATANBE M,et al.Secretion of small/microRNAs including miR-638 into extracellular spaces by sphingomyelin phosphodiesterase 3[J].Oncol Rep,2015,33(1):67-73.
[34] LIAO J,LIU R,SHI YJ,et al.Exosome-shuttling microRNA-21 promotes cell migration and invasion-targeting PDCD4 in esophageal cancer[J].Int J Oncol,2016,48(6):2567-2579.
[35] AL-RASHED F,AHMAD Z,THOMAS R,et al.Neutral sphingomyelinase 2 regulates inflammatory responses in monocytes/macrophages induced by TNF-α[J].Sci Rep,2020,10(1):16802.
[36] KARAKASHIAN AA,GILTIAV NV,SMITH GM,et al.Expression of neutral sphingomyelinase-2 (NSMase-2) in primary rat hepatocytes modulates IL-beta-induced JNK activation[J].FASEB J,2004,18(9):968-970.

Memo

Memo:
National Natural Science Foundation of China(No.81773766);国家自然科学基金(编号:81773766)
Last Update: 1900-01-01