Downregulation of Astrocyte Elevated Gene-1 Expression Combined with All-Trans Retinoic Acid Inhibits Development of Vasculogenic Mimicry and Angiogenesis in Glioma

Chen Liang , Ling Yang , Shi-wen Guo , Rui-chun Li

Current Medical Science ›› 2022, Vol. 42 ›› Issue (2) : 397 -406.

PDF
Current Medical Science ›› 2022, Vol. 42 ›› Issue (2) : 397 -406. DOI: 10.1007/s11596-022-2517-4
Article

Downregulation of Astrocyte Elevated Gene-1 Expression Combined with All-Trans Retinoic Acid Inhibits Development of Vasculogenic Mimicry and Angiogenesis in Glioma

Author information +
History +
PDF

Abstract

Objective

This study aimed to investigate the effects of downregulating astrocyte elevated gene-1 (AEG-1) expression combined with all-trans retinoic acid (ATRA) on vasculogenic mimicry (VM) formation and angiogenesis in glioma.

Methods

U87 glioma cells were transfected with AEG-1 shRNA lentiviral vectors (U87-siAEG-1) and incubated in a medium containing 20 µmol/L ATRA. Matrigel-based tube formation assay was performed to evaluate VM formation, and the cell counting kit-8 (CCK-8) assay was used to analyze the proliferation of glioma cells in vitro. Reverse transcription-quantitative polymerase chain reaction and Western blot analysis were used to investigate the mRNA and protein expression of related genes, respectively. Glioma xenograft models were generated via subcutaneous implantation of glioma cells in nude mice. Tumor-bearing mice received an intraperitoneal injection of ATRA (10 mg/kg per day). Immunohistochemistry was used to evaluate the expression of related genes and the microvessel density (MVD) in glioma xenograft models. CD34/periodic acid-Schiff double staining was performed to detect VM channels in vivo. The volume and weight of tumors were measured, and a tumor growth curve was drawn to evaluate tumor growth.

Results

A combination of ATRA intervention and downregulation of AEG-1 expression significantly inhibited the proliferation of glioma cells in vitro and glioma VM formation in vitro and in vivo. It also significantly decreased MVD and inhibited tumor growth. Further, the expression levels of matrix metalloproteinase (MMP)-2, MMP-9, vascular endothelial-cadherin (VE-cadherin), and vascular endothelial growth factor (VEGF) in glioma significantly decreased in vivo and in vivo.

Conclusion

Hence, a combinatorial approach might be effective in treating glioma through regulating MMP-2, MMP-9, VEGF, and VE-cadherin expression.

Keywords

astrocyte elevated gene-1 / glioma / all-trans retinoic acid / vasculogenic mimicry / angiogenesis

Cite this article

Download citation ▾
Chen Liang, Ling Yang, Shi-wen Guo, Rui-chun Li. Downregulation of Astrocyte Elevated Gene-1 Expression Combined with All-Trans Retinoic Acid Inhibits Development of Vasculogenic Mimicry and Angiogenesis in Glioma. Current Medical Science, 2022, 42(2): 397-406 DOI:10.1007/s11596-022-2517-4

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

TaylorOG, BrzozowskiJS, SkeldingKA. Glioblastoma Multiforme: An Overview of Emerging Therapeutic Targets. Front Oncol, 2019, 9: 963

[2]

KomoriT. The 2016 WHO Classification of Tumours of the Central Nervous System: The Major Points of Revision. Neurol Med Chir (Tokyo), 2017, 57(7): 301-311

[3]

LiY, HouM, LuG, et al.. The Prognosis of Anti-Angiogenesis Treatments Combined with Standard Therapy for Newly Diagnosed Glioblastoma: A Meta-Analysis of Randomized Controlled Trials. PLoS One, 2016, 11(12): e0168264

[4]

El HallaniS, BoisselierB, PeglionF, et al.. A new alternative mechanism in glioblastoma vascularization: tubular vasculogenic mimicry. Brain, 2010, 133: 973-982 Pt 4

[5]

ChenYS, ChenZP. Vasculogenic mimicry: a novel target for glioma therapy. Chin J Cancer, 2014, 33(2): 74-79

[6]

LiangC, GuoS, YangL. Effects of alltrans retinoic acid on VEGF and HIF1alpha expression in glioma cells under normoxia and hypoxia and its antiangiogenic effect in an intracerebral glioma model. Mol Med Rep, 2014, 10(5): 2713-2719

[7]

LingGQ, LiuYJ, KeYQ, et al.. All-trans retinoic acid impairs the vasculogenic mimicry formation ability of U87 stem-like cells through promoting differentiation. Mol Med Rep, 2015, 12(1): 165-172

[8]

TangRH, LiangC, JianSG, et al.. The Effects of All-Trans Retinoic Acid on Vasculogenic Mimicry Formation Ability in CD133+Glioma Stem Cells and Its Mechanisms. J Biosci Med, 2017, 5: 42-54

[9]

SrivastavaJ, RobertsonCL, RajasekaranD, et al.. AEG-1 regulates retinoid X receptor and inhibits retinoid signaling. Cancer Res, 2014, 74(16): 4364-4377

[10]

LiuL, WuJ, YingZ, et al.. Astrocyte elevated gene-1 upregulates matrix metalloproteinase-9 and induces human glioma invasion. Cancer Res, 2010, 70(9): 3750-3759

[11]

DingZ, ZhangZ, JinX, et al.. Interaction with AEG-1 and MDM2 is associated with glioma development and progression and correlates with poor prognosis. Cell Cycle, 2019, 18(2): 143-155

[12]

YingZ, LiJ, LiM. Astrocyte elevated gene 1: biological functions and molecular mechanism in cancer and beyond. Cell Biosci, 2011, 1(1): 36

[13]

ZouM, ZhuW, WangL, et al.. AEG-1/MTDH-activated autophagy enhances human malignant glioma susceptibility to TGF-beta1-triggered epithelial-mesenchymal transition. Oncotarget, 2016, 7(11): 13122-13138

[14]

RajasekaranD, SrivastavaJ, EbeidK, et al.. Combination of Nanoparticle-Delivered siRNA for Astrocyte Elevated Gene-1 (AEG-1) and All-trans Retinoic Acid (ATRA): An Effective Therapeutic Strategy for Hepatocellular Carcinoma (HCC). Bioconjug Chem, 2015, 26(8): 1651-1661

[15]

FrancesconeRA, FaibishM, ShaoR. A Matrigel-Based Tube Formation Assay to Assess the Vasculogenic Activity of Tumor Cells. J Vis Exp, 2011, 55: 3040

[16]

WuHB, YangS, WengHY, et al.. Autophagy-induced KDR/VEGFR-2 activation promotes the formation of vasculogenic mimicry by glioma stem cells. Autophagy, 2017, 13(9): 1528-1542

[17]

GeH, LuoH. Overview of advances in vasculogenic mimicry — a potential target for tumor therapy. Cancer Manag Res, 2018, 10: 2429-2437

[18]

LiangC, YangL, GuoS. All-trans retinoic acid inhibits migration, invasion and proliferation, and promotes apoptosis in glioma cells in vitro. Oncol Lett, 2015, 9(6): 2833-2838

[19]

XuX, JiaR, ZhouY, et al.. Investigation of vasculogenic mimicry in sebaceous carcinoma of the eyelid. Acta Ophthalmol, 2010, 88(5): e160-164

[20]

ZhangZ, HanY, ZhangK, et al.. Investigation of vasculogenic mimicry in intracranial hemangiopericytoma. Mol Med Rep, 2011, 4(6): 1295-1298

[21]

RobertsonFM, SimeoneAM, LucciA, et al.. Differential regulation of the aggressive phenotype of inflammatory breast cancer cells by prostanoid receptors EP3 and EP4. Cancer, 2010, 116(11Suppl): 2806-2814

[22]

HendrixMJ, SeftorEA, HessAR, et al.. Vasculogenic mimicry and tumour-cell plasticity: lessons from melanoma. Nat Rev Cancer, 2003, 3(6): 411-421

[23]

SeftorRE, SeftorEA, KoshikawaN, et al.. Cooperative interactions of laminin 5 gamma2 chain, matrix metalloproteinase-2, and membrane type-1-matrix/metalloproteinase are required for mimicry of embryonic vasculogenesis by aggressive melanoma. Cancer Res, 2001, 61(17): 6322-6327

[24]

LingL, ChenL, ZhangC, et al.. High glucose induces podocyte epithelialtomesenchymal transition by demethylationmediated enhancement of MMP9 expression. Mol Med Rep, 2018, 17(4): 5642-5651

[25]

FanYL, ZhengM, TangYL, et al.. A new perspective of vasculogenic mimicry: EMT and cancer stem cells (Review). Oncol Lett, 2013, 6(5): 1174-1180

[26]

HuangB, XiaoE, HuangM. MEK/ERK pathway is positively involved in hypoxia-induced vasculogenic mimicry formation in hepatocellular carcinoma which is regulated negatively by protein kinase A. Med Oncol, 2015, 32(1): 408

[27]

GuoJQ, ZhengQH, ChenH, et al.. Ginsenoside Rg3 inhibition of vasculogenic mimicry in pancreatic cancer through downregulation of VEcadherin/EphA2/MMP9/MMP2 expression. Int J Oncol, 2014, 45(3): 1065-1072

[28]

CaiHP, WangJ, XiSY, et al.. Tenascin-cmediated vasculogenic mimicry formation via regulation of MMP2/MMP9 in glioma. Cell Death Dis, 2019, 10(12): 879

[29]

HendrixMJ, SeftorEA, MeltzerPS, et al.. Expression and functional significance of VE-cadherin in aggressive human melanoma cells: role in vasculogenic mimicry. Proc Natl Acad Sci U S A, 2001, 98(14): 8018-8023

[30]

HessAR, SeftorEA, GrumanLM, et al.. VE-cadherin regulates EphA2 in aggressive melanoma cells through a novel signaling pathway: implications for vasculogenic mimicry. Cancer Biol Ther, 2006, 5(2): 228-233

[31]

WangJY, SunT, ZhaoXL, et al.. Functional significance of VEGF-a in human ovarian carcinoma: role in vasculogenic mimicry. Cancer Biol Ther, 2008, 7(5): 758-766

[32]

XuX, ZongY, GaoY, et al.. VEGF Induce Vasculogenic Mimicry of Choroidal Melanoma through the PI3k Signal Pathway. Biomed Res Int, 2019, 2019: 3909102

[33]

LiuY, LiF, YangYT, et al.. IGFBP2 promotes vasculogenic mimicry formation via regulating CD144 and MMP2 expression in glioma. Oncogene, 2018, 38(11): 1815-1831

[34]

QinL, RenY, ChenAM, et al.. Peroxisome proliferator-activated receptor gamma ligands inhibit VEGF-mediated vasculogenic mimicry of prostate cancer through the AKT signaling pathway. Mol Med Rep, 2014, 10(1): 276-282

[35]

MeiJ, GaoY, ZhangL, et al.. VEGF-siRNA silencing induces apoptosis, inhibits proliferation and suppresses vasculogenic mimicry in osteosarcoma in vitro. Exp Oncol, 2008, 30(1): 29-34

[36]

MaZ, ChenY, DongS, et al.. AEG-1 mRNA expression in non-small cell lung cancer is associated with increased tumor angiogenesis. Pathol Res Pract, 2017, 213(10): 1257-1263

[37]

HuangLL, WangZ, CaoCJ, et al.. AEG-1 associates with metastasis in papillary thyroid cancer through upregulation of MMP2/9. Int J Oncol, 2017, 51(3): 812-822

AI Summary AI Mindmap
PDF

86

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/