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1.
Eur Cell Mater ; 30: 248-57, 2015 Nov 12.
Article in English | MEDLINE | ID: mdl-26562631

ABSTRACT

Repair of dental pulp and periodontal lesions remains a major clinical challenge. Classical dental treatments require the use of specialised tissue-adapted materials with still questionable efficacy and durability. Stem cell-based therapeutic approaches could offer an attractive alternative in dentistry since they can promise physiologically improved structural and functional outcomes. These therapies necessitate a sufficient number of specific stem cell populations for implantation. Dental mesenchymal stem cells can be easily isolated and are amenable to in vitro expansion while retaining their stemness. In vivo studies realised in small and large animals have evidenced the potential of dental mesenchymal stem cells to promote pulp and periodontal regeneration, but have also underlined new important challenges. The homogeneity of stem cell populations and their quality control, the delivery method, the quality of the regenerated dental tissues and their integration to the host tissue are some of the key challenges. The use of bioactive scaffolds that can elicit effective tissue repair response, through activation and mobilisation of endogenous stem cell populations, constitutes another emerging therapeutic strategy. Finally, the use of stem cells and induced pluripotent cells for the regeneration of entire teeth represents a novel promising alternative to dental implant treatment after tooth loss. In this mini-review, we present the currently applied techniques in restorative dentistry and the various attempts that are made to bridge gaps in knowledge regarding treatment strategies by translating basic stem cell research into the dental practice.


Subject(s)
Dental Pulp/cytology , Regeneration/physiology , Stem Cells/cytology , Tissue Engineering , Tooth/cytology , Animals , Humans , Tissue Engineering/methods , Tissue Scaffolds
2.
Int J Androl ; 33(6): 765-74, 2010 Dec.
Article in English | MEDLINE | ID: mdl-20497259

ABSTRACT

Testicular germ cell tumours (TGCTs) represent about 2% of male malignancies, being the most common cancer among adolescents and young adults. As in most neoplasias, TGCTs show a chaotic vascular architecture, altered blood supply and over-expression of pro-angiogenic factors, aspects closely related to tumour overgrowth and metastasis. Following this trend, our laboratory has analysed the effect of the hypoxic tumour microenvironment on cancer stem cells, particularly the expression of factors related to vascularization, such as matrix metalloproteinases, adhesion molecules, vascular endothelial growth factors (VEGF) and VEGF receptors. This review also summarizes our present knowledge on vascularization in the normal and neoplastic testis, the potential role of the factors involved in TGCT neovascularization and their importance as possible therapeutic targets.


Subject(s)
Neoplasms, Germ Cell and Embryonal/blood supply , Neovascularization, Pathologic , Teratocarcinoma/blood supply , Testicular Neoplasms/blood supply , Adolescent , Adult , Angiogenesis Inhibitors/therapeutic use , Animals , Biomarkers, Tumor/blood , Cadherins/physiology , Cell Adhesion Molecules/physiology , Embryonic Stem Cells/transplantation , Humans , Integrins/physiology , Male , Matrix Metalloproteinase 14/physiology , Matrix Metalloproteinases/physiology , Neoplasm Metastasis/physiopathology , Testicular Neoplasms/pathology , Testis/blood supply , Vascular Endothelial Growth Factor A/physiology
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