ФИЗИОЛОГИЧЕСКАЯ СИСТЕМА СОЕДИНИТЕЛЬНОЙ ТКАНИ И ОНКОГЕНЕЗ. IV. МЕЗЕНХИМАЛЬНАЯ СТВОЛОВАЯ КЛЕТКА: ЧТО ОПРЕДЕЛЯЕТ НЕОДНОЗНАЧНОСТЬ ЕЕ ДЕЙСТВИЯ?

Автор(и)

  • Н.М. Бережная Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України, Київ, Україна
  • В.Ф. Чехун Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України, Київ, Україна

Ключові слова:

система соединительной ткани, онкогенез, мезенхимальная стволовая клетка, миграция, микроокружение, стимуляция роста опухоли, ангиогенез, иммуносупрессия, ниши, эпителиально-мезенхимальный переход, везикулы, miRNs.

Анотація

Мезенхимальная стволовая клетка (MSC) обладает рядом свойств, отличающих ее от других клеток соединительной ткани, может оказывать разнонаправленное влияние (стимуляция и ингибиция) на опухолевый рост. Втоже
время MSC сейчас достаточно широко используются для лечения ряда заболеваний, в том числе неонкологических. Учитывая изложенное, целью данного обзора явилось направленное рассмотрение роли и механизмов участия
MSC в развитии злокачественных новообразований. Проанализированы современные данные о тропизме MSC и ее миграции в микроокружение опухоли, влиянии на опухолевый рост (включая формирование ниш), на ангиогенез
и иммунологические процессы (в отношении которых проявляется преимущественно супрессивное действие). Рассмотрено значение MSC и их везикул в эпителиально-мезенхимальном переходе, изменение свойств опухолевых
клеток и характера роста опухоли (интенсивность пролиферации, метастазирования). Обсуждаются вопросы гетерогенности MSC, а также влияния микроокружения на их функционирование. Подчеркивается, что роль
MSC в опухолевом процессе выходит за рамки микроокружения. Постулировано, что сформированные в настоящее время представления об участии
MSC в опухолевом росте достаточно противоречивы, что обосновывает
настороженность в отношении последствий клинического использования
MSC и необходимость выработки дополнительных критериев для применения этих клеток в терапии.

Посилання

Chekhun VF, Berezhnaya NM. Physiological system of conjunctive tissue and oncogenesis. I. Role of cellular components

of stroma in tumor development. Оncology 2016; 18 (1): 4–12

(in Russian).

Chekhun VF, Berezhnaya NM. Physiological system of conjunctive tissue and oncogenesis. II. Extracellular matrix and metastasis. ІІ. Оncology 2016; 18 (3): 164–76 (in Russian).

Chekhun VF, Berezhnaya NM. Physiological system of conjunctive tissue and oncogenesis. III. Formation of resistance to chemotherapy. Oncology 2017; 19 (3): 156–70 (in Russian).

Liang L, Li Z, Ma T, et al. Transplantation of human placenta-derived mesenchymal stem cells alleviates critical limb ischemia in

diabetic nude rats. Cell Transplant 2017; 26 (1): 45–61.

Hill BS, Pelagalli A, Passaro N, Zannetti A. Tumor-educated

mesenchymal stem cells promote pro-metastatic phenotype. Oncotarget 2017; 8 (42): 73296–311.

Shi Q, Gao J, Jiang Y, et al. Differentiation of human umbilical cord Wharton's jelly-derived mesenchymal stem cells into endometrial cells. Stem Cell Res Ther 2017; 8 (1): 246.

Ehnert S, van Griensven M, Unger M, et al. Co-culture with

human osteoblasts and exposure to extremely low frequency pulsed

electromagnetic fields improve osteogenic differentiation of human

adipose-derived mesenchymal stem cells. Int J Mol Sci 2018; 19 (4):

pii. E994.

Moon MY, Kim HJ, Choi BY, et al. Promotes adipose-derived

mesenchymal stem cell proliferation and differentiation towards a neuronal fate. Stem Cells Int 2018; 2018: 5736535.

Sassoli C, Vallone L, Tani A, et al. Combined use of bone

marrow-derived mesenchymal stromal cells (BM-MSCs) and

platelet rich plasma (PRP) stimulates proliferation and differentiation of myoblasts in vitro: new therapeutic perspectives for

skeletal muscle repair/regeneration. Cell Tissue Res 2018; 372

(3): 549–70.

Barui A, Chowdhury F, Pandit A, Datta P. Rerouting mesenchymal stem cell trajectory towards epithelial lineage by engineering

cellular niche. Biomaterials 2018; 156: 28–44.

Talwadekar M, Fernandes S, Kale V, Limaye L. Valproic acid

enhances the neural differentiation of human placenta derived-mesenchymal stem cells in vitro. J Tissue Eng Regen Med 2017; 11 (11):

–23.

Zhang YM, Zhang ZM, Guan QL, et al. Co-culture with lung

cancer A549 cells promotes the proliferation and migration of mesenchymal stem cells derived from bone marrow. Exp Ther Med 2017;

(4): 2983–91.

Li L, Dong L, Hui J, et al. Under-expression of LATS1 promotes the differentiation, proliferation and migration of mesenchymal

stem cells by inhibition the Hippo signaling pathway in vitro. Zhonghua Wei Zhong Bing Ji Jiu Yi Xue 2017; 29 (8): 731–7.

Poggi A, Giuliani M. Mesenchymal stromal cells can regulate

the immune response in the tumor microenvironment. Vaccines (Basel) 2016; 4 (4): pii. E41.

Heissig B, Dhahri D, Eiamboonsert S, et al. Role of mesenchymal stem cell-derived fibrinolytic factor in tissue regeneration and

cancer progression. Cell Mol Life Sci 2015; 72 (24): 4759–70.

Kim J, Ko J. A novel PPARγ2 modulator sLZIP controls the

balance between adipogenesis and osteogenesis during mesenchymal

stem cell differentiation. Cell Death Differ 2014; 21 (10): 1642–55.

Fellows CR, Matta C, Zakany R, et al. Adipose, bone marrow and synovial joint-derived mesenchymal stem cells for cartilage

repair. Front Genet 2016; 7: 213.

Alessio N, Özcan S, Tatsumi K, et al. The secretome of

MUSE cells contains factors that may play a role in regulation of

stemness, apoptosis and immunomodulation. Cell Cycle 2017; 16

(1): 33–44.

Kishi T, Mayanagi T, Iwabuchi S, et al. Myocardin-related

transcription factor A (MRTF-A) activity-dependent cell adhesion is

correlated to focal adhesion kinase (FAK) activity. Oncotarget 2016;

(44): 72113–30.

Zhang R, Wang N, Zhang M, et al. Rho/MRTF-A-induced

integrin expression regulates angiogenesis in differentiated multipotent

mesenchymal stem cells. Stem Cells Int 2015; 2015: 534758.

Borriello L, Nakata R, Sheard MA, et al. Cancer-associated

fibroblasts share characteristics and protumorigenic activity with mesenchymal stromal cells. Cancer Res 2017; 77 (18): 5142–57.

Quante M, Tu SP, Tomita H, et al.Bone marrow-derived myofibroblasts contribute to the mesenchymal stem cell niche and promote tumor growth. Cancer Cell 2011; 19 (2): 257–72.

Ki-Jong Rhee, Jong In Lee, Young Woo Eom. Mesenchymal

stem cell-mediated effects of tumor support or suppression. Int J Mol

Sci 2015; 16 (12): 30015–33.

Dwyer RM, Potter-Beirne SM, Harrington KA, et al. Monocyte chemotactic protein-1 secreted by primary breast tumors stimulates migration of mesenchymal stem cells. Clin Cancer Res 2007;

: 5020–7.

Tang Y, Chen Y, Wang X, et al. Combinatorial intervention with

mesenchymal stem cells and granulocyte colony-stimulating factor in

a rat model of ulcerative colitis. Dig Dis Sci 2015; 60 (7): 1948–57.

Guan SP, Lam ATL, Newman JP, et al. Matrix metalloproteinase-1 facilitates MSC migration via cleavage of IGF-2/IGFBP2

complex. FEBS Open Bio 2017; 8 (1): 15–26.

Spaeth E, Klopp A, Dembinski J, et al.Inflammation and tumor microenvironments: defining the migratory itinerary of mesenchymal stem cells. Gene Ther 2008; 15 (10): 730–8.

Wang Z, Wang Y, Wang Z, et al. Engineered mesenchymal

stem cells with enhanced tropism and paracrine secretion of cytokines and growth factors to treat traumatic brain injury. Stem Cells

; 33 (2): 456–67.

Liu L, Chen JX, Zhang XW, et al. Chemokine receptor 7

overexpression promotes mesenchymal stem cell migration and

proliferation via secreting chemokine ligand 12. Sci Rep 2018; 8

(1): 204.

Bai L, Shao H, Wang H, et al. Effects of mesenchymal stem

cell-derived exosomes on experimental autoimmune uveitis. Sci Rep

; 7 (1): 4323.

Bayo J, Real A, Fiore EJ, et al. IL-8, GRO and MCP-1 produced by hepatocellular carcinoma microenvironment determine

the migratory capacity of human bone marrow-derived mesenchymal stromal cells without affecting tumor aggressiveness. Oncotarget

; 8 (46): 80235–48.

Chen YW, Hsieh SC, Yang YC, et al. Functional engineered

mesenchymal stem cells with fibronectin-gold composite coated

catheters for vascular tissue regeneration. Nanomedicine 2018; 14

(3): 699–711.

Lin SY, Dolfi SC, Amiri S, et al. P53 regulates the migration

of mesenchymal stromal cells in response to the tumor microenvironment through both CXCL12-dependent and -independent mechanisms. Int J Oncol 2013; 43 (6): 1817–23.

Berger L, Shamai Y, Skorecki KL, Tzukerman M. Tumor specific recruitment and reprogramming of mesenchymal stem cells in

tumorigenesis. Stem Cells 2016; 34 (4): 1011–26.

Uchibori R, Tsukahara T, Mizuguchi H, et al. NF-κB activity

regulates mesenchymal stem cell accumulation at tumor sites. Cancer Res 2013; 73 (1): 364–72.

Kalluri R. The biology and function of fibroblasts in cancer.

Nat Rev Cancer 2016; 16 (9): 582–98.

Weber CE, Kothari AN, Wai PY, et al. Osteopontin mediates an MZF1-TGF-β1-dependent transformation of mesenchymal

stem cells into cancer-associated fibroblasts in breast cancer. Oncogene 2015; 34 (37): 4821–33.

Yuan Z, Kolluri KK, Sage EK, et al.Mesenchymal stromal cell

delivery of full-length tumor necrosis factor-related apoptosis-inducing ligand is superior to soluble type for cancer therapy. Cytotherapy

; 17 (7): 885–96.

Melzer C, Yang Yu, Hass R. Interaction of MSC with tumor

cells. Cell Commun Signal 2016; 14 (1): 20.

Touboul C, Vidal F, Pasquier J, et al. Role of mesenchymal

cells in the natural history of ovarian cancer: a review. J Transl Med

; 12: 271.

Wang LL, Yu Y, Guan HB, Qiao C. Effect of human umbilical cord mesenchymal stem cell transplantation in a rat model of preeclampsia. Reprod Sci 2016; 23 (8): 1058–70.

Maffioli E, Nonnis S, Angioni R, et al. Proteomic analysis of

the secretome of human bone marrow-derived mesenchymal stem

cells primed by pro-inflammatory cytokines. J Proteomics 2017; 166:

–26.

Dang RJ, Yang YM, Zhang L, et al. A20 plays a critical role

in the immunoregulatory function of mesenchymal stem cells. J Cell

Mol Med 2016; 20 (8): 1550–60.

Nwabo Kamdje AH, Kamga PT, Simo RT, et al.Mesenchymal

stromal cells’ role in tumor microenvironment: involvement of signaling pathways. Cancer Biol Med 2017; 14 (2): 129–41.

Wang Y, Xu J, Zhang X, et al. TNF-α-induced LRG1 promotes angiogenesis and mesenchymal stem cell migration in the

subchondral bone during osteoarthritis. Cell Death Dis 2017; 8

(3): e2715.

Zhang T, Lee YW, Rui YF, et al. Bone marrow-derived mesenchymal stem cells promote growth and angiogenesis of breast and

prostate tumors. Stem Cell Res Ther 2013; 4 (3): 70.

Zhou SL, Zheng C, Su JQ, et al. Isolation and identification

of human umbilical cord and placenta-derived stem cells and their

component analysis. Zhongguo Shi Yan Xue Ye Xue Za Zhi 2015;

(6): 1684–91.

Tian K, Yang S, Ren Q, et al. p38 MAPK contributes to the

growth inhibition of leukemic tumor cells mediated by human umbilical cord mesenchymal stem cells. Cell Physiol Biochem 2010; 26

(6): 799–808.

Bajetto A, Pattarozzi A, Corsaro A, et al. Different effects of

human umbilical cord mesenchymal stem cells on glioblastoma stem

cells by direct cell interaction or via released soluble factors. Front Cell

Neurosci 2017; 11: 312.

Ciria M, García NA, Ontoria-Oviedo I, González-King H, et

al. Mesenchymal stem cell migration and proliferation are mediated

by hypoxia-inducible factor-1α upstream of notch and sumo pathways. Stem Cells Dev 2017; 26 (13): 973–85.

Pakravan K, Babashah S, Sadeghizadeh M, et al. MicroRNA-100 shuttled by mesenchymal stem cell-derived exosomes

suppresses in vitro angiogenesis through modulating the mTOR/

HIF-1α/VEGF signaling axis in breast cancer cells. Cell Oncol

(Dordr) 2017; 40 (5): 457–70.

Yi D, Xiang W, Zhang Q, et al. Human glioblastoma-derived

mesenchymal stem cell to pericytes transition and angiogenic capacity in glioblastoma microenvironment. Cell Physiol Biochem 2018;

(1): 279–90.

Gong M, Yu B, Wang J, et al. Mesenchymal stem cells release

exosomes that transfer miRNAs to endothelial cells and promote angiogenesis. Oncotarget 2017; 8 (28): 45200–12.

Liang X, Zhang L, Wang S, et al. Exosomessecreted by mesenchymal stem cells promote endothelial cell angiogenesis by transferring miR-125a. J Cell Sci 2016; 129 (11): 2182–9.

Wang Q, Zhang Z, Ding T, et al. Mesenchymal stem cells overexpressing PEDF decrease the angiogenesis of gliomas. Biosci Rep

; 33 (2): e00019.

Chaturvedi P, Gilkes DM, Takano N, Semenza GL. Hypoxiainducible factor-dependent signaling between triple-negative breast

cancer cells and mesenchymal stem cells promotes macrophage recruitment. Proc Natl Acad Sci USA 2014; 111 (20): E2120–9.

Hagenhoff A, Bruns CJ, Zhao Y, et al. Harnessing mesenchymal stem cell homing as an anticancer therapy. Expert Opin Biol Ther

; 16 (9): 1079–92.

Chen HW, Chen HY, Wang LT, et al.Mesenchymal stem cells

tune the development of monocyte-derived dendritic cells toward

a myeloid-derived suppressive phenotype through growth-regulated

oncogene chemokines. J Immunol 2013; 190 (10): 5065–77.

Wang Q, Ding G, Xu X. Immunomodulatory functions of mesenchymal stem cells and possible mechanisms. Histol Histopathol

; 31 (9): 949–59.

Melzer C, von der Ohe J, Hass R. Enhanced metastatic capacity of breast cancer cells after interaction and hybrid formation

with mesenchymal stroma/stem cells (MSC). Cell Commun Signal 2018; 16: 2.

Bassi ÊJ, de Almeida DC, Moraes-Vieira PM, Câmara NO.

Exploring the role of soluble factors associated with immune regulatory properties of mesenchymal stem cells. Stem Cell Rev 2012; 8

(2): 329–42.

De Miguel MP, Fuentes-Julián S, Blázquez-Martínez A, et al.

Immunosuppressive properties of mesenchymal stem cells: advances

and applications. Curr Mol Med 2012; 12 (5): 574–91.

Haddad R, Saldanha-Araujo F. Mechanisms of T-cell immunosuppression by mesenchymal stromal cells: what do we know so

far? Biomed Res Int 2014; 2014: 216806.

Cordeiro MF, Marmitt LP, Horn AP. Subcutaneous injection of multipotent mesenchymal stromal cells admixed with

melanoma cells in mice favors tumor incidence and growth: a systematic review and meta-analysis. Arch Dermatol Res 2018; 310

(3): 231–240.

Duffy MM, Ritter T, Ceredig R, Griffin MD. Mesenchymal stem cell effects on T-cell effector pathways. Stem Cell Res Ther

; 2 (4): 34.

Burgler S, Mantel PY, Bassin C, et al. RORC2 is involved in

T cell polarization through interaction with the FOXP3 promoter. J

Immunol 2010; 184 (11): 6161–9.

Gottschling S, Granzow M, Kuner R, et al.Mesenchymal stem

cells in non-small cell lung cancer-different from others? Insights

from comparative molecular and functional analyses. Lung Cancer

; 80 (1): 19–29.

Yu Y, Xiao CH, Tan LD, et al.Cancer-associated fibroblasts induce epithelial-mesenchymal transition of breast cancercells through

paracrine TGF-β signalling. Br J Cancer 2014; 110 (3): 724–32.

Galland S, Vuille J, Martin P, Letovanec I, et al. Tumorderived mesenchymal stem cells use distinct mechanisms to block

the activity of natural killer cell subsets. Cell Rep 2017; 20 (12):

–905.

Lu Y, Liu J, Liu Y, et al. TLR4 plays a crucial role in MSCinduced inhibition of NK cell function. Biochem Biophys Res Commun 2015; 464 (2): 541–7.

Zhu Q, Zhang X, Zhang L, et al. The IL-6-STAT3 axis mediates a reciprocal crosstalk between cancer-derived mesenchymal stem

cells and neutrophils to synergistically prompt gastric cancer progression. Cell Death Dis 2014; 5 (6): e1295.

Yang T, Zhang X, Wang M, et al. Activation of mesenchymal

stem cells by macrophages prompts human gastric cancer growth

through NF-κB pathway. PLoS One 2014; 9 (5): e97569.

Zhang Q, Fu L, Liang Y, et al. Exosomes originating from

MSCs stimulated with TGF-β and IFN-γ promote Treg differentiation. J Cell Physiol 2018; 233 (9): 6832–40.

Kota DJ, DiCarlo B, Hetz RA, et al. Differential MSC activation leads to distinct mononuclear leukocyte binding mechanisms.

Sci Rep 2014; 4: 4565.

Hu X, Zhou Y, Dong K, et al. Programming of the development of tumor-promoting neutrophils by mesenchymal stromal cells.

Cell Physiol Biochem 2014; 33 (6): 1802–14.

Poggi A, Varesano S, Zocchi MR. How to hit mesenchymal

stromal cells and make the tumor microenvironment immunostimulant rather than immunosuppressive. Front Immunol 2018; 9: 262.

Bach M, Schimmelpfennig C, Stolzing A. Influence of murine

mesenchymal stem cells on proliferation, phenotype, vitality, and cytotoxicity of murine cytokine-induced killer cells in coculture. PLoS

One 2014; 9 (2): e88115.

Laranjeira P, Pedrosa M, Pedreiro S, et al. Effect of human

bone marrow mesenchymal stromal cells on cytokine production by

peripheral blood naive, memory, and effector T cells. Stem Cell Res

Ther 2015; 6 (1): 3.

Davies LC, Heldring N, Kadri N, Le Blanc K. Mesenchymal

stromal cell secretion of programmed death-1 ligands regulates T cell

mediated immunosuppression. Stem Cells 2017; 35 (3): 766–76.

Rosado MM, Bernardo ME, Scarsella M, et al. Inhibition of

B-cell proliferation and antibody production by mesenchymal stromal cells is mediated by T cells. Stem Cells Dev 2015; 24 (1): 93–103.

Ji YR, Yang ZX, Han ZB, et al. Mesenchymal stem cells support proliferation and terminal differentiation of B cells. Cell Physiol

Biochem 2012; 30 (6): 1526–37.

Di Trapani M, Bassi G, Midolo M, et al.Differential and transferable modulatory effects of mesenchymal stromal cell-derived extracellular vesicles on T, B and NK cell functions. Sci Rep 2016; 6: 24120.

Mezey É, Nemeth K. Mesenchymal stem cells and infectious

diseases: Smarter than drugs. Immunol Lett 2015; 168 (2): 208–14.

Dostert G, Mesure B, Menu P, Velot É. How do mesenchymal

stem cells influence or are influenced by microenvironment through

extracellular vesicles communication? Front Cell Dev Biol 2017; (5): 6.

Yang Y, Bucan V, Baehre H, et al. Acquisition of new tumor

cell properties by MSC-derived exosomes. Int J Oncol 2015; 47 (1):

–52.

Bruno S, Collino F, Deregibus MC, et al. Microvesicles derived from human bone marrow mesenchymal stem cells inhibit tumor growth. Stem Cells Dev 2013; 22: 758–71.

Heldring N, Mäger I, Wood MJ, et al. Therapeutic potential of multipotent mesenchymal stromal cells and their extracellular vesicles. Hum Gene Ther 2015; 26 (8): 506–17.

Shi S, Zhang Q, Xia Y, et al. Mesenchymal stem cell-derived exosomes facilitate nasopharyngeal carcinoma progression.

Am J Cancer Res 2016; 6 (2): 459–72.

Bruno S, Deregibus MC, Camussi G. The secretome of mesenchymal stromal cells: Role of extracellular vesicles in immunomodulation. Immunol Lett 2015; 168 (2): 154–8.

Lee JK, Park SR, Jung BK, et al.Exosomesderived from mesenchymal stem cells suppress angiogenesis by down-regulating VEGF

expression in breast cancer cells. PLoS One 2013; 8 (12): e84256.

Chowdhury R, Webber JP, Gurney M, et al.Cancer exosomes

trigger mesenchymal stem cell differentiation into pro-angiogenic and pro-invasive myofibroblasts. Oncotarget 2015; 6 (2): 715–31.

Gu J, Qian H, Shen L, et al. Gastric cancer exosomes trigger differentiation of umbilical cord derived mesenchymal stem cells

to carcinoma-associated fibroblasts through TGF-β/SMAD pathway. PLoS One 2012; 7: e52465.

Cho JA, Park H, Lim EH, Lee KW. Exosomes from breast

cancer cells can convert adipose tissue-derived mesenchymal stem

cells into myofibroblast-like cells. Int J Oncol 2012; 40 (1): 130–8.

Lozito TP, Tuan RS. Endothelial and cancer cells interact with

mesenchymal stem cells via both microparticles and secreted factors.

J Cell Mol Med 2014; 18 (12): 2372–84.

Wang S, Huang S, Sun YL. Epithelial-mesenchymal transition

in pancreatic cancer: a review. Biomed Res Int 2017; 2017: 2646148.

Wu F, Zhu J, Mao Y, et al.Associations between the epithelial-mesenchymal transition phenotypes of circulating tumor cells and

the clinicopathological features of patients with colorectal cancer. Dis

Markers 2017; 2017: 9474532.

Zhang X, Hu F, Li G, et al. Human colorectal cancer-derived mesenchymal stem cells promote colorectal cancer progression through IL-6/JAK2/STAT3 signaling. Cell Death Dis 2018;

(2): 25.

Klopp AH, Lacerda L, Gupta A, et al.Mesenchymal stem cells

promote mammosphere formation and decrease E-cadherin in normal

and malignant breast cells. PLoS One 2010; 5 (8): e12180.

Iser IC, Ceschini SM, Onzi GR, et al. Conditioned medium

from adipose-derived stem cells (adscs) promotes epithelial-to-mesenchymal-like transition (emt-like) in glioma cells in vitro. Mol Neurobiol 2016; 53 (10): 7184–99.

Ly C, Dai H, Sun M, et al. Mesenchymal stem cells induce epithelial mesenchymal transition in melanoma by paracrine

secretion of transforming growth factor-β. Melanoma Res 2017; 27

(2): 74–84.

Giannoni E, Bianchini F, Masieri L, et al. Reciprocal activation of prostate cancer cells and cancer-associated fibroblasts stimulates epithelial-mesenchymal transition and cancer stemness. Cancer

Res 2010; 70 (17): 6945–56.

Laurenzana A, Biagioni A, Bianchini F, et al. Inhibition

of uPAR-TGFβ crosstalk blocks MSC-dependent EMT in melanoma cells. J Mol Med (Berl) 2015; 93 (7): 783–94.

Gupta R, Chetty C, Bhoopathi P, et al. Downregulation of

uPA/uPAR inhibits intermittent hypoxia-induced epithelial-mesenchymal transition (EMT) in DAOY and D283 medulloblastoma cells.

Int J Oncol 2011; 38 (3): 733–44.

Wu HJ, Yiu WH, Li RX, et al.Mesenchymal stem cells modulate albumin-induced renal tubular inflammation and fibrosis. PLoS

One 2014; 9 (3): e90883.

So KA, Min KJ, Hong JH, Lee JK. Interleukin-6 expression

by interactions between gynecologic cancer cells and human mesenchymal stem cells promotes epithelial-mesenchymal transition. Int J

Oncol 2015; 47 (4): 1451–9.

Mele V, Muraro MG, Calabrese D, et al. Mesenchymal

stromal cells induce epithelial-to-mesenchymal transition in human colorectal cancer cells through the expression of surface-bound

TGF-β. Int J Cancer 2014; 134 (11): 2583–94.

Luo D, Hu S. Mesenchymal stem cells promote cell invasion and migration and autophagy-induced epithelial-mesenchymal

transition in A549 lung adenocarcinoma cells. Cell Biochem Funct

; 36 (2): 88–94.

Martin FT, Dwyer RM, Kelly J, et al. Potential role of mesenchymal stem cells (MSCs) in the breast tumour microenvironment:

stimulation of epithelial to mesenchymal transition (EMT). Breast

Cancer Res Treat 2010; 124 (2): 317–26.

Song L, Zhou X, Jia HJ, et al. Effect of hGC-MSCs from

human gastric cancer tissue on cell proliferation, invasion and epithelial-mesenchymal transition in tumor tissue of gastric cancer

tumor-bearing mice. Asian Pac J Trop Med 2016; 9 (8): 796–800.

Chiabotto G, Bruno S, Collino F, Camussi G. Mesenchymal stromal cells epithelial transition induced by renal tubular cellsderived extracellular vesicles. PLoS One 2016; 11 (7): e0159163.

Mani SA, Guo W, Liao MJ, et al. The epithelial-mesenchymal transition generates cells with properties of stem cells. Cell

; 133 (4): 704–15.

Banyard J, Bielenberg DR. The role of EMT and MET in

cancer dissemination. Connect Tissue Res 2015; 56 (5): 403–13.

Jolly MK, Ware KE, Gilja S, et al. EMT and MET: necessary or permissive for metastasis? Mol Oncol 2017; 11 (7): 755–69.

Ju JA, Godet I, Ye IC, et al. Hypoxia selectively enhances

integrin α5β1 receptor expression in breast cancer to promote metastasis. Mol Cancer Res 2017; 15 (6): 723–34.

El Marsafy S, Larghero J. Mesenchymal stem cells: key actors in tumor niche. Curr Stem Cell Res Ther 2015; 10 (6): 523–9.

Krstic J, Trivanovic D, Jaukovic A, et al. Metabolic plasticity of stem cells and macrophages in cancer. Front Immunol

; 8: 939.

Melzer C, von der Ohe J, Lehnert H, et al. Cancer stem cell

niche models and contribution by mesenchymal stroma/stem cells.

Mol Cancer 2017; 16: 28.

Seke Etet PF, Vecchio L, Bogne Kamga P, et al. Normal hematopoiesis and hematologic malignancies: role of canonical Wnt

signaling pathway and stromal microenvironment. Biochim Biophys

Acta 2013; 1835 (1): 1–10.

Nwabo Kamdje AH, Seke Etet PF, et al. New targeted therapies for breast cancer: A focus on tumor microenvironmental signals and chemoresistant breast cancers. World J Clin Cases 2014; 2

(12): 769–86.

Seke Etet PF, Vecchio L, Nwabo Kamdje AH. Interactions between bone marrow stromal microenvironment and B-chronic lymphocytic leukemia cells: any role for Notch, Wnt and Hh signaling

pathways? Cell Signal 2012; 24 (7): 1433–43.

Maeda K, Enomoto A, Hara A, et al. Identification of meflin as a potential marker for mesenchymal stromal cells. Sci Rep

; 6: 22288.

Corcoran KE, Trzaska KA, Fernandes H, et al. Mesenchymal stem cells in early entry of breast cancer into bone marrow. PLoS

One 2008; 3 (6): e2563.

Hou L, Wang X, Zhou Y, et al. Inhibitory effect and mechanism of mesenchymal stem cells on liver cancer cells. Tumour Biol

; 35 (2): 1239–50.

Nakata R, Shimada H, Fernandez GE, et al. Contribution of

neuroblastoma-derived exosomes to the production of pro-tumorigenic signals by bone marrow mesenchymal stromal cells. J Extracell

Vesicles 2017; 6 (1): 1332941.

Jakubikova J, Cholujova D, Hideshima T, et al. A novel 3D

mesenchymal stem cell model of the multiple myeloma bone marrow niche: biologic and clinical applications. Oncotarget 2016; 7

(47): 77326–41.

von der Heide EK, Neumann M, Vosberg S, et al. Molecular alterations in bone marrow mesenchymal stromal cells derived from acute myeloid leukemia patients. Leukemia 2017; 31

(5): 1069–8.

Kim JA, Shim JS, Lee GY, et al. Microenvironmental remodeling as a parameter and prognostic factor of heterogeneous leukemogenesis in acute myelogenous leukemia. Cancer Res 2015; 75

(11): 2222–31.

Secchiero P, Zorzet S, Tripodo C, et al. Human bone marrow mesenchymal stem cells display anti-cancer activity in SCID mice

bearing disseminated non-Hodgkin’s lymphoma xenografts. PLoS

One 2010; 5 (6): e11140.

Böhrnsen F, Fricke M, Sander C, et al.Interactions of human

MSC with head and neck squamous cell carcinoma cell line PCI-13

reduce markers of epithelia-mesenchymal transition. Clin Oral Investig 2015; 19 (5): 1121–8.

Clarke MR, Imhoff FM, Baird SK. Mesenchymal stem cells

inhibit breast cancer cell migration and invasion through secretion of

tissue inhibitor of metalloproteinase-1 and -2. Mol Carcinogen 2015;

(10): 1214–9.

Luo J, Lee SO, Cui Y, et al. Infiltrating bone marrow mesenchymal stem cells (BM-MSCs) increase prostate cancer cell invasion via altering the CCL5/HIF2α/androgen receptor signals. Oncotarget 2015; 6 (29): 27555–65.

DeBerardinis RJ, Chandel NS. Fundamentals of cancer metabolism. Sci Adv 2016; 2 (5): e1600200.

He X, Wang H, Jin T, et al. TLR4 activation promotes bone

marrow MSC proliferation and osteogenic differentiation via Wnt3a

and Wnt5a signaling. PLoS One 2016; 11 (3): e0149876.

Zgheib A, Pelletier-Bonnier É, Levros LC Jr, Annabi B. Selective JAK/STAT3 signalling regulates transcription of colony stimulating factor-2 and -3 in Concanavalin-A-activated mesenchymal

stromal cells. Cytokine 2013; 63 (2): 187–93.

Waterman RS, Henkle SL, Betancourt AM. Mesenchymal

stem cell 1 (MSC1)-based therapy attenuates tumor growth whereas MSC2-treatment promotes tumor growth and metastasis. PLoS

One 2012; 7 (9): e45590.

Dabrowski FA, Burdzinska A, Kulesza A, et al. Comparison

of the paracrine activity of mesenchymal stem cells derived from human umbilical cord, amniotic membrane and adipose tissue. J Obstet Gynaecol Res 2017; 43 (11): 1758–68.

Li L, Tian H, Chen Z, et al.Inhibition of lung cancer cell proliferation mediated by human mesenchymal stem cells. Acta Biochim

Biophys Sin (Shanghai) 2011; 43 (2): 143–8.

Hong IS, Lee HY, Kang KS. Mesenchymal stem cells and

cancer: friends or enemies? Mutat Res 2014; 768: 98–106.

Ridge SM, Sullivan FJ, Glynn SA. Mesenchymal stem cells:

key players in cancer progression. Mol Cancer 2017; 16 (1): 31.

Melzer C, von der Ohe J, Hass R. Concise review: Crosstalk

of mesenchymal stroma/stem-like cells with cancer cells provides therapeutic potential. Stem Cells 2018. doi: 10.1002/stem.2829.

Daquinag AC, Tseng C, Zhang Y, et al. Targeted proapoptotic peptides depleting adipose stromal cells inhibit tumor growth. Mol

Ther 2016; 24 (1): 34–40.

Lou G, Song X, Yang F, et al. Exosomes derived from miR122-modified adipose tissue-derived MSCs increase chemosensitivity

of hepatocellular carcinoma. J Hematol Oncol 2015; 8: 122.

Lin R, Wang S, Zhao RC. Exosomes from human adiposederived mesenchymal stem cells promote migration through Wnt signaling pathway in a breast cancer cell model. Mol Cell Biochem 2013;

(1–2): 13–20.

Timari H, Shamsasenjan K, Movassaghpour A, et al.The effect of mesenchymal stem cell-derived extracellular vesicles on hematopoietic stem cells fate. Adv Pharm Bull 2017; 7 (4): 531–46.

Barberini DJ, Freitas NP, Magnoni MS, et al. Equine mesenchymal stem cells from bone marrow, adipose tissue and umbilical

cord: immunophenotypic characterization and differentiation potential. Stem Cell Res Ther 2014; 5 (1): 25.

Huang L, Niu C, Willard B, et al. Proteomic analysis of porcine mesenchymal stem cells derived from bone marrow and umbilical cord: implication of the proteins involved in the higher migration capability of bone marrow mesenchymal stem cells. Stem Cell

Res Ther 2015; 6: 77.

Zhang X, Tu H, Yang Y, et al.Mesenchymal stem cell-derived

extracellular vesicles: roles in tumor growth, progression, and drug resistance. Stem Cells Int 2017; 2017: 1758139.

Khan M, Adil SE, Olson AL. The role of mesenchymal stem

cells in oncology and regenerative medicine. Future Oncol 2017; 13

(9): 821–31.

Yang X, Hou J, Han Z, et al. One cell, multiple roles: contribution of mesenchymal stem cells to tumor development in tumor

microenvironment. Cell Biosci 2013; 3 (1): 5.

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Опубліковано

2018-07-11

Як цитувати

Бережная, Н., & Чехун, В. (2018). ФИЗИОЛОГИЧЕСКАЯ СИСТЕМА СОЕДИНИТЕЛЬНОЙ ТКАНИ И ОНКОГЕНЕЗ. IV. МЕЗЕНХИМАЛЬНАЯ СТВОЛОВАЯ КЛЕТКА: ЧТО ОПРЕДЕЛЯЕТ НЕОДНОЗНАЧНОСТЬ ЕЕ ДЕЙСТВИЯ?. Oncology, 20(2), 77–92. вилучено із https://nasu-periodicals.org.ua/index.php/oncology/article/view/26908

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