International Journal of Biomedical and Clinical Sciences
Articles Information
International Journal of Biomedical and Clinical Sciences, Vol.6, No.3, Sep. 2021, Pub. Date: Aug. 20, 2021
Role of Chronic Psychological Stress in microRNA Biogenesis and microRNA Regulated Signal Transduction Pathways During Cancer
Pages: 80-91 Views: 966 Downloads: 187
Authors
[01] Mohammad Rakibul Alam, Department of Molecular Medicine, Kyungpook National University, Daegu, Republic of Korea.
[02] Mohammad Rubayet Ahsan, Biotechnology and Genetic Engineering Discipline, Khulna University, Khulna, Bangladesh.
[03] Rezowan Kabir, Biomedical Engineering Department, Military Institute of Science and Technology (MIST), Mirpur Cantonment, Dhaka, Bangladesh.
[04] Sourav Biswas Nayan, Department of Food Engineering, North Pacific International University of Bangladesh, Manikganj, Bangladesh.
[05] Mahbub E. Sobhani, Biotechnology and Genetic Engineering Discipline, Khulna University, Khulna, Bangladesh.
Abstract
The role of RNA in the central dogma of life has been changed after the discovery of evolutionary conserved, single stranded petite RNA molecule named microRNA (miRNA). miRNA is an essential regulator of gene expression that controls both physiological and pathological process in the progression of cancer. In order to reveal the role of miRNA, we have studied major signalling pathways including: IGF1R, AKT, MAPK, and WNT pathways. miRNA has significant role in activating these pathways as well as down-regulating apoptotic proteins i.e. PTEN, FOXO, p 53, p 21, p 27, puma, Bim, GSK3β, AXIN, APC, CK1α, RUNX3, SOX, NLK and up-regulating oncogenic proteins i.e. Ras, VEGF, ctnnB. During chronic psychological stress, body elevates the production of glucocorticoids (GCs) via hypothalamic pituitary adrenocortical (HPA) axis which ultimately facilitates tumorigenesis through regulation of signal transduction pathways. Binding with Glucocorticoid receptor, GCs activates the oncogenic transcription factor c-Myc that binds directly to the E-box sequence of Drosha promoter to produce mature miRNA and eventually leads cellular proliferation and cancer development. This paper reviews chronic psychological stress induced GCs secretion, and propose molecular mechanism of GCs regulated mature miRNA production and miRNA mediated regulation of cellular signal transduction pathways during cancer.
Keywords
Chronic Psychological Stress, Glucocorticoid, miRNA Biogenesis, IGF1R/AKT/MAPK/WNT Signalling Pathways
References
[01] Sandi C, Haller J. Stress and the social brain: behavioural effects and neurobiological mechanisms. Nat. Rev. Neurosci. (2015); 16: 290-304.
[02] Dai S, Mo Y, Wang Y, Xiang B, et al. Chronic Stress Promotes Cancer Development. Front. Oncol. (2020); 10: 1492.
[03] Menard C, Pfau ML, Hodes GE, Kana V, Wang VX, et al. Social stress induces neurovascular pathology promoting depression. Nat. Neurosci. (2017); 20: 1752-60.
[04] Fidler MM, Gupta S, Soerjomataram I, Ferlay J, et al. Cancer incidence and mortality among young adults aged 20-39 years worldwide in 2012: a population-based study. Lancet Oncol. (2017); 18: 1579-89.
[05] Cui B, Luo Y, Tian P, Peng F, et al. Stress-induced epinephrine enhances lactate dehydrogenase A and promotes breast cancer stem-like cells. J. Clin. Invest. (2019); 129: 1030-46.
[06] Zhang X, Zhang Y, He Z, Yin K, et al. Chronic stress promotes gastric cancer progression and metastasis: an essential role for ADRB2. Cell Death Dis. (2019); 10: 788.
[07] Olejniczak M, Kotowska-Zimmer A, Krzyzosiak W. Stress-induced changes in microRNA biogenesis and functioning. Cell. Mol. Life Sci. (2018); 75: 177-191
[08] Treiber T, Treiber N, Meister G. Regulation of microRNA biogenesis and its crosstalk with other cellular pathways. Nat. Rev. Mol. Cell Biol. (2019); 20: 5-20.
[09] MacFarlane LA, Murphy PR. MicroRNA: Biogenesis function and fole in cancer. Current Genomics. (2010); 11: 537-561.
[10] Friedman RC, Farth KK, Burge CB, Bartel DP. Most mammalian mRNAs are conserved targets of MicroRNA. J. Genome Res. (2009); 19: 92-105.
[11] Feng Z. p53 Regulation of the IGF-1/AKT/mTOR Pathways and the Endosomal Compartment. Cold Spring Harb Perspect Biol. (2010); 2: a001057.
[12] Laplante M, Sabatini DM. mTOR signaling at a glance. Journal of Cell Science. (2009); 122: 3589-3594.
[13] Roma J, an-Moga AA, Toledo JS, Gallego S. Notch, Wnt, and Hedgehog Pathways in Rhabdomyosarcoma: from Single Pathways to an Integrated Network. Sarcoma. (2012); doi: 10.1155/695603.
[14] Xu M, Mo YY. The Akt-associated microRNAs. Cell Mol. Life Sci. (2012); 69: 3601-3612.
[15] Ahsan MR, Rafat AMA, Sobhani ME, Molla MAW. Biomolecular basis of the role of chronic psychological stress hormone ‘‘glucocorticoid’’ in alteration of cellular immunity during cancer. Memo. (2013); 6: 127-136.
[16] Yuan A, Wang S, li Z, Huang C. Psychological aspect of cancer: From stressor to cancer progression (Review). Experimental and therapeutic medicine. (2010); 1: 13-18.
[17] Wang X, Zhao X, Gao P, Wu M. c-Myc modulate microRNA processing via the transcriptional regulation of Drosha. Scientific Report. (2013); 3: 1942.
[18] Lee Y, Ahn C, Han J, Choi H, et al. The nuclear RNase III Drosha initiates microRNA processing. Nature. (2003); 425: 415-419.
[19] Antoni MH, Lutgendorf SK, Cole SW, Dhabhar FS, et al. The influence of bio-behavioural factors on tumour biology: pathways and mechanisms. Nat. Rev. Cancer. (2006); 6: 240-248.
[20] Thaker PH, LY Han, Kamat AA, Arevalo JM, et al. Chronic stress promotes tumor growth and angiogenesis in a mouse model of ovarian carcinoma. Nat. Med. (2004); 12: 939-944.
[21] Sood AK, Bhatty R, Kamat AA, Landen CN, et al. Stress hormone-mediated invasion of ovarian cancer cells. Clin. Cancer Res. (2006); 12: 369-375.
[22] Lutgendorf SK, Cole S, Costanzo E, Bradley S, et al. Stress-related mediators stimulate vascular endothelial growth factor secretion by two ovarian cancer cell lines. Clin. Cancer Res. (2003); 9: 4514-4521.
[23] Drube S, Stirnweiss J, Valkova C, Liebmann C. Ligand independent and EGF receptor-supported transactivation: lessons from beta2-adrenergic receptor signalling. Cell Signal. (2006); 18: 1633-1646.
[24] Kerkvliet CP, Dwyer AR, Diep CH, Oakley RH, et al. Glucocorticoid receptors are required effectors of TGFB-1 induced p38 MAPK signaling to advanced cancer phenotypes in triple-negative breast cancer. Breast Cancer Research. (2020); 22: 39.
[25] Petrella A, Ercolino SF, Festa M, Gentilella A, et al. Dexamethasone inhibits trailinduced apoptosis of thyroid cancer cells via Bcl-xL induction. Eur J. Cancer. (2006); 42: 3287-3293.
[26] Wang JC, Derynck MK, Nonaka DF, Khodabakhsh DB, et al. Chromatin immunoprecipitation (ChIP) scanning identifies primary glucocorticoid receptor target genes. Proc. Natl. Acad. Sci. (2004); 101: 15603-15608.
[27] Fu L, Lee CC. The circadian clock: pacemaker and tumour suppressor. Nat. Rev. Cancer. (2003); 3: 350-361.
[28] Deng G, Sui G. Noncoding RNA in Oncogenesis: A New Era of Identifying Key Players. International Journal of Molecular Science. (2013); 14: 18319-18349.
[29] Bertone P, Stolc V, Royce TE, Rozowsky JS, et al. Global identification of human transcribed sequences with genome tiling arrays. Science. (2004); 306: 2242-2246.
[30] Wilusz JE, Sunwoo H, Spector DL. Long noncoding RNAs: Functional surprises from the RNA world. Genes Dev. (2009); 23: 1494-1504.
[31] Mercer TR, Dinger ME, Mattick JS. Long non-coding RNAs: Insights into functions. Nat. Rev. Genet. (2009); 10: 155-159.
[32] Lagos-Quintana M, Rauhut R, Meyer J, Borkhardt A, et al. New microRNAs from mouse and human. RNA. (2003); 9: 175-179.
[33] Farh KK, Grimson A, Jan C, Lewis BP, et al. The widespread impact of mammalian microRNAs on mRNA repression and evolution. Science (2005); 310: 1817-1821.
[34] Eulalio A, Huntzinger E, Izaurralde E. Getting to the Root of miRNA-Mediated Gene Silencing. Cell. (2008); 132: 1-14.
[35] Fernandez N, Cordiner RA, Young RS, Hug N, et al. Genetic variation and RNA structure regulate microRNA biogenesis. Nat. Commun. (2017); 8: 15114.
[36] O’Brien J, Hayder H, Zayed Y, Peng C. Overview of microRNA biogenesis, mechanism of actions and circulation. Front. in Endocrinol. (2019); 9: 402.
[37] Hwanga HW, Wentzel EA, Mendell JT. Cell–cell contact globally activates microRNA biogenesis. PNAS. (2009); 106: 7016-7021.
[38] Krol J, Loedige I, Filipowicz W. The widespread regulation of microRNA biogenesis, function and decay. Nat. Rev. Genet. (2010); 11: 597-610.
[39] Frank F, Sonenberg N, Nagar B. Structural basis for 5′-nucleotide base-specific recognition of guide RNA by human AGO2. Nature. (2010); 465: 818-822.
[40] Filipowicz W, Bhattacharyya SN, Sonenberg N. Mechanisms of post-transcriptional regulation by microRNAs: are the answers in sight? Nat. Rev. Genet. (2008); 9: 102-114.
[41] Kiriakidou M, Tan GS, Lamprinaki S, De Planell-Saguer M, et al. An mRNA m7G cap binding-like motif within human Ago2 represses translation. Cell. (2007); 129: 1141-1151.
[42] Chendrimada TP, Finn KJ, Ji X, Baillat D. MicroRNA silencing through RISC recruitment of eIF6. Nature. (2007); 447: 823–828.
[43] Liu J, Rivas FV, Wohlschlegel J, Yates JR, Parker R, Hannon GJ. A role for the P-body component GW182 in microRNA function. Nat. Cell Biol. (2005); 7: 1261–1266.
[44] Robbins and Cotran. Neoplasia. In: Kumar V, Abbas AK, Fausto N, Aster JC, editors. Pathologic basis of disease. Pennsylvania: Elsevier; 2010. p. 259-330.
[45] Ma T, Copland JA, Brasier AR, Thompson EA. A novel glucocorticoid receptor binding element within the murin c-myc promoter. Mol. Endocrinol. (2000); 14 (9): 1377-1386.
[46] Haisa M. The type 1 insulin-like growth factor receptor signalling system and targeted tyrosine kinase inhibition in cancer. Journal of International Medical Research. (2013); 41: 253-264.
[47] Knowlton DL, Tang K, Henstock PV, Subramanian RR. miRNA Alterations Modify Kinase Activation In The IGF-1 Pathway And Correlate With Colorectal Cancer Stage And Progression In Patients. Journal of Cancer. (2011); 2: 490-502.
[48] Chitnis MM, Yuen JSP, Protheroe AS, Pollak M, Macaulay VM. The Type 1 Insulin-Like Growth Factor Receptor Pathway. Clin. Cancer Res.( 2008); 14: 6364-6370.
[49] Xiao C, Srinivasan L, Calado D P, Patterson HC, et al. Lymphoproliferative disease and autoimmunity in mice with increased miR-17-92 expression in lymphocytes. Nat. Immunol. (2008); 9: 405-414.
[50] Poliseno L, Salmena L, Riccardi L, Fornari A, et al. Identification of the miR-106b-25 microRNA cluster as a proto-oncogenic PTEN targeting intron that cooperates with its host gene MCM7 in transformation. Science Signaling. (2010); doi: 10.1126/2000594.
[51] Meng F, Henson R, Wehbe-janek H, Ghoshal K, et al. MicroRNA-21 regulates expression of the PTEN tumor suppressor gene in human hepatocellular cancer. Gastroenterology. (2007); 133: 647-658.
[52] Mavrakis KJ, Meulen JVD, Wolfe AL, Liu X, et al. A cooperative microRNA-tumor suppressor gene network in acute T-cell lymphoblastic leukemia. Nat. Genet. (2011); 43: 815-826.
[53] Wang C, Bian Z, Wei D, Zhang JG. miR-29b regulates migration of human breast cancer cells. Molecular and Cellular Biochemistry. (2011); 352: 197-207.
[54] Yang H, Kong W, He L, Zhao AA, et al. MicroRNA expression profiling in human ovarian cancer: miR-214 induces cell survival and cisplatin resistance by targeting PTEN. Cancer Research. (2008); 68: 1609-1618.
[55] Kato M, Putta S, Wang M, Yuan H, et al. TGF-β β activates Akt kinase through a microRNA-dependent amplifying circuit targeting PTEN. Nat. Cell Biol. (2009); 11: 881-889.
[56] Incoronato M, Garofalo M, Urso L, Romano G, et al. miR-212 increases tumor necrosis factor-related apoptosis-inducing ligand sensitivity in non-small cell lung cancer by targeting the antiapoptotic protein PED. Cancer Research. (2010); 70: 3638–3646.
[57] Garofalo M, Di Leva G, Romano G, Nuovo G, et al. miR-221 & 222 Regulate TRAIL Resistance and Enhance Tumorigenicity through PTEN and TIMP3 Downregulation. Cancer Cell. (2009); 16: 498-509.
[58] Wu W, Yang J, Feng X, Wang H, et al. MicroRNA-32 (miR-32) regulates phosphatase and tensin homologue (PTEN) expression and promotes growth, migration, and invasion in colorectal carcinoma cells. Molecular Cancer. (2013); 12: 1-11.
[59] Ma J, Liu J, Wang Z, Gu X, et al. NF-kappaB-dependent MicroRNA-425 upregulation promotes gastric cancer cell growth by targeting PTEN upon IL-1β induction. Molecular Cancer. (2014); 13: 1-11.
[60] Zhang LY, Ho-Fun Lee V, Wong AM, Kwong DL, et al. MicroRNA-144 promotes cell proliferation, migration and invasion in nasopharyngeal carcinoma through repression of PTEN. Carcinogenesis. (2013); 34: 454-463.
[61] Lei L, Huang Y, Gong W. miR-205 promotes the growth, metastasis and chemoresistance of NSCLC cells by targeting PTEN. Oncology Reports. (2013); 30: 2897-2902.
[62] Dong P, Konno Y, Watari H, Hosaka M, et al. The impact of microRNA-mediated PI3K/AKT signaling on epithelial-mesenchymal transition and cancer stemness in endometrial cancer. Journal of Translational Medicine. (2014); 12: 1-9.
[63] Sachdeva M, Wu H, Ru P, Hwang L, et al. microRNA-101-mediated AKT activation and estrogen-independent growth. Oncogene. (2011); 30: 822-831.
[64] Zhou BP, and Hung MC. Novel targets of Akt, p21 (Cipl/WAF1), and MDM2. Semin Oncol. (2002); 29: 62-70.
[65] Sionov RV. MicroRNAs and Glucocorticoid-Induced Apoptosis in Lymphoid Malignancies. ISRN Hematology. (2013); doi.org/10.1155/348212.
[66] Croce C M. Causes and consequences of microRNA dysregulation in cancer. Nat. Rev. Genet. (2009); 10: 704-714.
[67] Sun M, Liu XH, Li JH, Yang JS, et al. MiR-196a is upregulated in gastric cancer and promotes cell proliferation by downregulating p27 kip1. Mol Cancer Ther. (2012); 11: 842-852.
[68] Hunten S, Siemens H, Kaller M, Hermeking H. The p53/microRNA network in cancer: Experimental and bioinformatics approaches. Adv. Exp. Med. Biol. (2013); 774: 77-101.
[69] Swarbrick A, Woods SL, Shaw A, Balakrishnan A, et al. miR-380-5p represses p53 to control cellular survival and is associated with poor outcome in MYCN-amplified neuroblastoma. Nat. Med. (2010); 16: 1134-1140.
[70] Guttilla I K, and White B A. Coordinate regulation of FOXO1 by miR-27a, miR-96, and miR-182 in breast cancer cells. The Journal of Biological Chemistry. (2009); 284: 23204-23216.
[71] Elia L, Contu R, Quintavalle M, Varrone F, et al. Reciprocal regulation of microrna-1 and insulin-like growth factor-1 signal transduction cascade in cardiac and skeletal muscle in physiological and pathological conditions. Circulation. (2009); 120: 2377-2385.
[72] Yamamoto M, Kondo E, Takeuchi M, Harashima A, et al. miR-155, a modulator of FOXO3a protein expression, is under expressed and cannot be upregulated by stimulation of HOZOT, a line of multifunctional Treg. PLoS ONE. (2011); 6: e16841.
[73] Wagner EF and Nebreda AR. Signal integration by JNK and p38 MAPK pathways in cancer development. Nat. Rev. Cancer. (2009); 9: 537-549.
[74] Sun D, Yu F, Ma Y, Zhao R, et al. MicroRNA-31 Activates the RAS Pathway and Functions as an Oncogenic MicroRNA in Human Colorectal Cancer by Repressing RAS p21 GTPase Activating Protein 1 (RASA1). Journal of Biological Chemistry. (2013); 288: 9508-9518.
[75] Lemmon MA, Schlessinger J. Cell signaling by receptor tyrosine kinases. Cell. (2010); 141: 1117-1134.
[76] Sun X, He Y, Huang C, Ma TT, Li J. Distinctive microRNA signature associated of neoplasms with the Wnt/β-catenin signaling pathway. Cellular Signalling. (2013); 25: 2805-2811.
[77] Xi S, Yang M, Tao T, Xu H, et al. Cigarette smoke induces C/EBP-β-mediated activation of miR-31 in normal human respiratory epithelia and lung cancer cells. PLoS One. (2010); 5: e13764.
[78] Cai J, Guan H, Fang L, Yang Y, et al. MicroRNA-374a activates Wnt/β-catenin signaling to promote breast cancer metastasis. Clin. Invest. (2013); 123: 566-579.
[79] Zhang LL, Liu JJ, Liu F, Liu WH, et al. MiR-499 induces cardiac differentiation of rat mesenchymal stem cells through wnt/β-catenin signaling pathway. Biochem. Biophys. Res. Commun. (2012); 420: 875-881.
[80] Zhang X, Li M, Zuo K, Li D, et al. Upregulated miR-155 in papillary thyroid carcinoma promotes tumor growth by targeting APC and activating Wnt/β-catenin signaling. Clin Endocrinol. Metab. (2013); 98: 1305-1313.
[81] Egea V, Zahler S, Rieth N, Neth P, et al. Tissue inhibitor of metalloproteinase-1 (TIMP1) regulates mesenchymal stem cells through let-7f microRNA and Wnt/β-catenin signaling. Proc. Natl. Acad. Sci. (2012); 109: 309-316.
[82] Silver SJ, Hagen JW, Okamura K, Perrimon N, Lai EC. Functional screening identifies miR-315 as a potent activator of Wingless signaling. Proc. Natl. Acad. Sci. (2007); 104: 18151-18156.
[83] Ma L, Young J, Prabhala H, Pan E, et al. miR-9, a MYC/MYCN-activated microRNA, regulates E-cadherin and cancer metastasis. Nat. cell Biol. (2010); 12: 247-258.
[84] Zhang P, Bill K, Liu J, Young E, et al. MiR-155 is a liposarcoma oncogene that targets casein kinase-1α and enhances β-catenin signaling. Cancer Res. (2012); 72: 1751-1762.
[85] Ito K, Lim AC, Tellez MS, Motoda L, et al. RUNX3 Attenuatesb-Catenin/T Cell Factors in Intestinal Tumorigenesis. Cancer Cell. (2008); 14: 226-237.
[86] Wang K, Wang X, Zou J, Zhang A, et al. miR-92b controls glioma proliferation and invasion through regulating Wnt/beta-catenin signaling via Nemo-like kinase. Neuro-Oncol. (2013); 15: 578-588.
[87] Katoh M, Katoh M. WNT signaling pathway and stem cell signaling network. Clinical Cancer Research. (2007); 13: 4042-4045.
[88] Lin CY, Loven J, Rahl PB, Paranal RM, et al. Transcriptional Amplification in Tumor Cells with Elevated c-Myc. Cell. (2012); 151: 56-67.
[89] Mestdagh P, Fredlund E, Pattyn F, Schulte JH, et al. MYCN/c-MYC-induced microRNAs repress coding gene networks associated with poor outcome in MYCN/c-MYC-activated tumors. Oncogene. (2010); 29: 1394-1404.
[90] Donnell KAO, Wentzel EA, Zeller KI, Dang CV, Mendell JT. c-Myc-regulated microRNAs modulate E2F1 Expression. Nature. (2005); 435: 839-843.
[91] Chang TC, Yu D, Lee Y, Wentzel EA, et al. Widespread microRNA repression by Myc contributes to tumorigenesis. Nat. Genet. (2008); 40: 43-50.
[92] Dews M, Homayouni A, Yu D, Murphy D, et al. Augmentation of tumor angiogenesis by a Myc-activated microRNA cluster. Nat. Genet. (2006); 38: 1060-1065.
600 ATLANTIC AVE, BOSTON,
MA 02210, USA
+001-6179630233
AIS is an academia-oriented and non-commercial institute aiming at providing users with a way to quickly and easily get the academic and scientific information.
Copyright © 2014 - American Institute of Science except certain content provided by third parties.