|Table of Contents|

Targeting SHMT2 to up-regulate the expression of ESR1 enhances the anti-breast cancer effect of tamoxifen

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

Issue:
2024 20
Page:
3834-3840
Research Field:
Publishing date:

Info

Title:
Targeting SHMT2 to up-regulate the expression of ESR1 enhances the anti-breast cancer effect of tamoxifen
Author(s):
WANG Luwei1BI Xianxia1KONG Haoran2MO Fei2WANG Yingjie2HU Jinxia2QIN Yue1
1.Peninsula Cancer Center of Binzhou Medical University,Shandong Yantai 264003,China;2.Department of Biochemistry and Molecular Biology,Binzhou Medical College,Shandong Yantai 264003,China.
Keywords:
breast cancerSHMT2ESR1tamoxifenproliferationmigration
PACS:
R737.9
DOI:
10.3969/j.issn.1672-4992.2024.20.003
Abstract:
Objective:To investigate the correlation between the expression of SHMT2 and ESR1 in breast cancer tissues,and to investigate the effect of targeting SHMT2 on the treatment of breast cancer with tamoxifen.Methods:The expression of SHMT2 in breast cancer cells was analyzed with online tools and verified by immunohistochemistry.The correlation and clinical significance of SHMT2 and ESR1 expression were analyzed.MCF-7 and T47D were selected as cell models,knock down of SHMT2 was performed using RNAi,SHMT2 activity was inhibited with small molecule compound SHIN2,qRT-PCR and Western blot were used to detect the expression of ESR1.Colony formation assay was carried for detect the effects of siRNA knockdown,tamoxifen treatment,or siRNA combined with tamoxifen on proliferation of breast cancer cells.Transwell assay was used to detect the effects of SHMT2 targeted inhibitors SHIN2,tamoxifen,and the combination of SHIN2 and tamoxifen treatment on cell migration.Results:Bioinformatics analysis revealed that SHMT2 was highly expressed in breast cancer tissues,and the higher expression of SHMT2 in ER positive breast cancer was correlated with poor prognosis of patients.Knockdown or inhibition of SHMT2 activity lead to the up-regulation of ESR1,and tamoxifen combined with siRNA or SHIN2 has a stronger inhibitory effect on the proliferation and migration of breast cancer cells.Conclusion:There is a negative correlation between the expression of SHMT2 and ESR1 in breast cancer tissue.Targeting or inhibiting of SHMT2 activity can up-regulate ESR1 expression and enhance the anti-breast cancer effect of tamoxifen.

References:

[1]Breast Cancer Expert Committee of National Cancer Quality Control C,Breast Cancer Expert Committee of China Anti-Cancer A,Cancer Drug Clinical Research Committee of China Anti-Cancer A.Guidelines for clinical diagnosis and treatment of advanced breast cancer in China (2022 edition) [J].Chinese Journal of Oncology,2022,44:1262-1287.
[2]LI X,ZHANG Y,ZHANG T,et al.Tafazzin mediates tamoxifen resistance by regulating cellular phospholipid composition in ER-positive breast cancer [J].Cancer Gene Ther,2024,31(1):69-81.
[3]BUIJS SM,VAN DORST D,KRUIP M,et al.The interplay between tamoxifen and endoxifen plasma concentrations and coagulation parameters in patients with primary breast cancer [J].Biomed Pharmacother,2024,170:115969.
[4]BARDIA A,IAFRATE JA,SUNDARESAN T,et al.Metastatic breast cancer with ESR1 mutation:Clinical management considerations from the molecular and precision medicine (MAP) tumor board at massachusetts general hospital [J].Oncologist,2016,21(9):1035-1040.
[5]BAHREINI A,LI Z,WANG P,et al.Mutation site and context dependent effects of ESR1 mutation in genome-edited breast cancer cell models [J].Breast Cancer Res,2017,19(1):60.
[6]GIANNOPOULOU L,MASTORAKI S,BUDERATH P,et al.ESR1 methylation in primary tumors and paired circulating tumor DNA of patients with high-grade serous ovarian cancer [J].Gynecol Oncol,2018,150(2):355-360.
[7]BOS MK,DEGER T,SLEIJFER S,et al.ESR1 methylation measured in Cell-Free DNA to evaluate endocrine resistance in metastatic breast cancer patients [J].Int J Mol Sci,2022,23(10):5631.
[8]KONG W,WANG Z,CHEN N,et al.SHMT2 regulates serine metabolism to promote the progression and immunosuppression of papillary renal cell carcinoma [J].Front Oncol,2022,12:914332.
[9]LI J,BO Y,DING B,et al.Understanding the regulatory role of USP32 and SHMT2 in the progression of gastric cancer [J].Cell J,2023,25(4):222-228.
[10]CUI X,CUI Y,DU T,et al.SHMT2 drives the progression of colorectal cancer by regulating UHRF1 expression [J].Can J Gastroenterol Hepatol,2022,2022:3758697.
[11]WU ZZ,WANG S,YANG QC,et al.Increased expression of SHMT2 is associated with poor prognosis and advanced pathological grade in oral squamous cell carcinoma [J].Front Oncol,2020,10:588530.
[12]ZHANG P,YANG Q.Overexpression of SHMT2 predicts a poor prognosis and promotes tumor cell growth in bladder cancer [J].Front Genet,2021,12:682856.
[13]CHEN L,LIU H,JI Y,et al.Downregulation of SHMT2 promotes the prostate cancer proliferation and metastasis by inducing epithelial-mesenchymal transition [J].Exp Cell Res,2022,415(2):113138.
[14]CHEN J,NA R,XIAO C,et al.The loss of SHMT2 mediates 5-fluorouracil chemoresistance in colorectal cancer by upregulating autophagy [J].Oncogene,2021,40(23):3974-3988.
[15]MAO Y,ZHANG T.Knockdown of SHMT2 enhances the sensitivity of gastric cancer cells to radiotherapy through the Wnt/beta-catenin pathway [J].Open Life Sci,2022,17(1):1249-1255.
[16]JIN X,LI L,PENG Q,et al.Glycyrrhetinic acid restricts mitochondrial energy metabolism by targeting SHMT2 [J].iScience,2022,25(5):104349.
[17]BERNHARDT S,BAYERLOVA M,VETTER M,et al.Proteomic profiling of breast cancer metabolism identifies SHMT2 and ASCT2 as prognostic factors[J].Breast Cancer Res,2017,19(1):112.
[18]ZHANG L,CHEN Z,XUE D,et al.Prognostic and therapeutic value of mitochondrial serine hydroxyl-methyltransferase 2 as a breast cancer biomarker[J].Oncol Rep,2016,36(5):2489-2500.
[19]USMAN M,HAMEED Y,AHMAD M,et al.SHMT2 is associated with tumor purity,CD8+ T immune cells infiltration,and a novel therapeutic target in four different human cancers[J].Curr Mol Med,2023,23(2):161-176.
[20]CHOI YJ,LEE G,YUN SH,et al.The role of SHMT2 in modulating lipid metabolism in hepatocytes via glycine-mediated mTOR activation [J].Amino Acids,2022,54(5):823-834.
[21]FIDDLER JL,BLUM JE,HEYDEN KE,et al.Impairments in SHMT2 expression or cellular folate availability reduce oxidative phosphorylation and pyruvate kinase activity [J].Genes Nutr,2023,18(1):5.
[22]LIU Z,FAN M,HOU J,et al.Serine hydroxymethyltransferase 2 knockdown induces apoptosis in ccRCC by causing lysosomal membrane permeabilization via metabolic reprogramming [J].Cell Death Dis,2023,14(2):144.
[23]LIAO Y,WANG F,ZHANG Y,et al.Silencing SHMT2 inhibits the progression of tongue squamous cell carcinoma through cell cycle regulation [J].Cancer Cell Int,2021,21(1):220.
[24]ZHANG Y,LIU Z,WANG X,et al.SHMT2 promotes cell viability and inhibits ROS-dependent,mitochondrial-mediated apoptosis via the intrinsic signaling pathway in bladder cancer cells [J].Cancer Gene Ther,2022,29(10):1514-1527.
[25]ZHANG H,CHE Y,XUAN B,et al.Serine hydroxymethyltransferase 2 (SHMT2) potentiates the aggressive process of oral squamous cell carcinoma by binding to interleukin enhancer-binding factor 2 (ILF2)[J].Bioengineered,2022,13(4):8785-8797.
[26]XIE SY,SHI DB,OUYANG Y,et al.SHMT2 promotes tumor growth through VEGF and MAPK signaling pathway in breast cancer [J].Am J Cancer Res,2022,12(7):3405-3421.
[27]QI C,QIN X,ZHOU Z,et al.Circ_0072995 promotes cell carcinogenesis via up-regulating miR-149-5p-mediated SHMT2 in breast cancer [J].Cancer Manag Res,2020,12:11169-11181.
[28]HUO FC,XIE M,ZHU ZM,et al.SHMT2 promotes the tumorigenesis of renal cell carcinoma by regulating the m6A modification of PPAT[J].Genomics,2022,114(4):110424.
[29]LIU C,WANG L,LIU X,et al.Cytoplasmic SHMT2 drives the progression and metastasis of colorectal cancer by inhibiting beta-catenin degradation [J].Theranostics,2021,11(6):2966-2986.
[30]MINTON DR,NAM M,MCLAUGHLIN DJ,et al.Serine catabolism by SHMT2 is required for proper mitochondrial translation initiation and maintenance of Formylmethionyl-tRNAs [J].Mol Cell,2018,69(4):610-621.
[31]ANDERSON DD,STOVER PJ.SHMT1 and SHMT2 are functionally redundant in nuclear de novo thymidylate biosynthesis [J].Plos One,2009,4(6):e5839.
[32]POULARD C,HA PT,DROUET Y,et al.Nuclear PRMT5 is a biomarker of sensitivity to tamoxifen in ERalpha(+) breast cancer [J].Embo Mol Med,2023,15(8):e17248.
[33]ZHANG H,WANG J,LI J,et al.HMGB1 is a key factor for tamoxifen resistance and has the potential to predict the efficacy of CDK4/6 inhibitors in breast cancer [J].Cancer Sci,2021,112(4):1603-1613.
[34]LI X,ZHANG K,HU Y,et al.ERRalpha activates SHMT2 transcription to enhance the resistance of breast cancer to lapatinib via modulating the mitochondrial metabolic adaption [J].Biosci Rep,2020,40(1):BSR20192465.

Memo

Memo:
National Natural Science Foundation of China(No.81502536);国家自然科学基金(编号:81502536);山东省自然科学基金面上项目(编号:ZR2020MH218,ZR2023MH367);山东省大学生科技创新项目(编号:S202310440199,S202210440046)
Last Update: 1900-01-01