References
- Rodrigues M, Kosaric N, Bonham CA, et al. Wound healing: a cellular perspective. Physiol Rev. 2019;99(1):665–706.
- Pastar I, Stojadinovic O, Tomic-Canic M. Role of keratinocytes in healing of chronic wounds. Surg Technol Int. 2008;17:105–112.
- Kim M, Kim J, Shin YK, et al. Gentisic acid stimulates keratinocyte proliferation through ERK1/2 phosphorylation. Int J Med Sci. 2020;17:626–631.
- Martinotti S, Ranzato E. Scratch wound healing assay. Methods Mol Biol. 2020;2109:225–229.
- Veith AP, Henderson K, Spencer A, et al. Therapeutic strategies for enhancing angiogenesis in wound healing. Adv Drug Deliv Rev. 2019;146:97–125.
- Bi Z, Liu Y, Zhao Y, et al. A dynamic reversible RNA N 6-methyladenosine modification: current status and perspectives. J Cell Physiol. 2019;234(6):7948–7956.
- Wang J, Chen L, Qiang P. The role of IGF2BP2, an m6A reader gene, in human metabolic diseases and cancers. Cancer Cell Int. 2021;21(1):99.
- Hou P, Meng S, Li M, et al. LINC00460/DHX9/IGF2BP2 complex promotes colorectal cancer proliferation and metastasis by mediating HMGA1 mRNA stability depending on m6A modification. J Exp Clin Cancer Res. 2021;40(1):52.
- Ma YS, Shi BW, Guo JH, et al. microRNA-320b suppresses HNF4G and IGF2BP2 expression to inhibit angiogenesis and tumor growth of lung cancer. Carcinogenesis. 2021;42(5):762–771.
- Wu Y, Zhong JL, Hou N, et al. MicroRNA Let-7b inhibits keratinocyte migration in cutaneous wound healing by targeting IGF2BP2. Exp Dermatol. 2017;26(2):116–123.
- Wu L, Davies GJ. An overview of the structure, mechanism and specificity of human heparanase. Adv Exp Med Biol. 2020;1221:139–167.
- Masola V, Gambaro G, Onisto M. Impact of heparanse on organ fibrosis. Adv Exp Med Biol. 2020;1221:669–684.
- Lv Q, Wu K, Liu F, et al. Interleukin17A and heparanase promote angiogenesis and cell proliferation and invasion in cervical cancer. Int J Oncol. 2018;53:1809–1817.
- Wang C, Wei Y, Wang G, et al. Heparanase potentiates the invasion and migration of pancreatic cancer cells via epithelial to mesenchymal transition through the Wnt/betacatenin pathway. Oncol Rep. 2020;44:711–721.
- Brant JO, Boatwright JL, Davenport R, et al. Comparative transcriptomic analysis of dermal wound healing reveals de novo skeletal muscle regeneration in acomys cahirinus. Plos One. 2019;14:e0216228.
- Li JH, Liu S, Zhou H, et al. starBase v2.0: decoding miRNA-ceRNA, miRNA-ncRNA and protein-RNA interaction networks from large-scale CLIP-Seq data. Nucleic Acids Res. 2014;42:D92–7.
- Bardou P, Mariette J, Escudie F, et al. jvenn: an interactive Venn diagram viewer. BMC Bioinformatics. 2014;15(1):293.
- Xie C, Mao X, Huang J, et al. KOBAS 2.0: a web server for annotation and identification of enriched pathways and diseases. Nucleic Acids Res. 2011;39(suppl_2):W316–22.
- Sun Z, Zhang A, Hou M, et al. Circular RNA hsa_circ_0000034 promotes the progression of retinoblastoma via sponging microRNA-361-3p. Bioengineered. 2020;11(1):949–957.
- Liu Z, Liu Q, Chen S, et al. Circular RNA Circ_0005564 promotes osteogenic differentiation of bone marrow mesenchymal cells in osteoporosis. Bioengineered. 2021;12(1):4911–4923.
- Sun Y, Hou ZQ, Luo BL, et al. Circular RNA circRNA_0082835 promotes progression and lymphatic metastasis of primary melanoma by sponging microRNA miRNA-429. Bioengineered. 2021;12(1):4159–4173.
- Liu Y, Yang F, Ma W, et al. Metformin inhibits proliferation and proinflammatory cytokines of human keratinocytes in vitro via mTOR-signaling pathway. Pharm Biol. 2016;54(7):1173–1178.
- Ren L, Lou Y, Sun M. The anti-tumor effects of evodiamine on oral squamous cell carcinoma (OSCC) through regulating advanced glycation end products (AGE) / receptor for advanced glycation end products (RAGE) pathway. Bioengineered. 2021;12(1):5985–5995.
- Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods. 2001;25:402–408.
- Wang X, Ji Y, Feng P, et al. The m6A reader IGF2BP2 regulates macrophage phenotypic activation and inflammatory diseases by stabilizing TSC1 and PPARγ. Adv Sci (Weinh). 2021;8(13):2100209.
- Zeng R, Lin C, Lin Z, et al. Approaches to cutaneous wound healing: basics and future directions. Cell Tissue Res. 2018;374:217–232.
- Shibata S, Tada Y, Asano Y, et al. Adiponectin regulates cutaneous wound healing by promoting keratinocyte proliferation and migration via the ERK signaling pathway. J Immunol. 2012;189:3231–3241.
- Du H, Zhou Y, Suo Y, et al. CCN1 accelerates re-epithelialization by promoting keratinocyte migration and proliferation during cutaneous wound healing. Biochem Biophys Res Commun. 2018;505:966–972.
- Chen X, Zhang M, Wang X, et al. Peptide-modified chitosan hydrogels promote skin wound healing by enhancing wound angiogenesis and inhibiting inflammation. Am J Transl Res. 2017;9:2352–2362.
- Hattori N, Mochizuki S, Kishi K, et al. MMP-13 plays a role in keratinocyte migration, angiogenesis, and contraction in mouse skin wound healing. Am J Pathol. 2009;175(2):533–546.
- Liu Y, Dong N, Miao J, et al. Lin28 promotes dental pulp cell proliferation via upregulation of cyclin-dependent proteins and interaction with let-7a/IGF2BP2 pathways. Biomed Pharmacother. 2019;113:108742.
- Ye S, Song W, Xu X, et al. IGF2BP2 promotes colorectal cancer cell proliferation and survival through interfering with RAF-1 degradation by miR-195. FEBS Lett. 2016;590(11):1641–1650.
- Li Y, Qiang W, Griffin BB, et al. HMGA2-mediated tumorigenesis through angiogenesis in leiomyoma. Fertil Steril. 2020;114(5):1085–1096.
- Johnson KE, Wilgus TA. Vascular endothelial growth factor and angiogenesis in the regulation of cutaneous wound repair. Adv Wound Care (New Rochelle). 2014;3(10):647–661.
- Cheng TL, Chen PK, Huang WK, et al. Plasminogen/thrombomodulin signaling enhances VEGF expression to promote cutaneous wound healing. J Mol Med (Berl). 2018;96:1333–1344.
- Hoss SG, Grundmann M, Benkel T, et al. Pro-angiogenic effects of latent heparanase and thrombin receptor-mediated pathways-do they share a common ground in melanoma cells? Thromb Haemost. 2018;118:1803–1814.
- Wang XL, Niu YJ, Ma JM. [HIF-1alpha, HPSE and VEGF promote malignant progression of retinoblastoma]. Zhonghua Yan Ke Za Zhi. 2010;46:140–144.
- Carmel J, Arish A, Shoshany G, et al. Heparanase accelerates the proliferation of both hepatocytes and endothelial cells early after partial hepatectomy. Exp Mol Pathol. 2012;92(2):202–209.