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Updated: Feb 18, 2026

Fabrication of Tongue Extracellular Matrix and Reconstitution of Tongue Squamous Cell Carcinoma In Vitro
Published on: June 20, 2018
Dental Pulp Stem Cell-Derived Secretome-Induced Reprogramming of Tongue Tumor Microenvironment.
Ferry Sandra1,2, Dewi Ranggaini3, Johni Halim3
1Department of Biochemistry and Molecular Biology, Division of Oral Biology, Faculty of Dentistry, Universitas Trisakti, Indonesia.
Dental pulp stem cell-derived secretome (DPSC-Sec) shows promise for reprogramming the tumor microenvironment (TME) in oral tongue cancer. This approach may overcome therapy resistance by modulating key TME components.
Area of Science:
- Oncology
- Stem Cell Biology
- Cancer Microenvironment Research
Background:
- Oral tongue cancer is aggressive, with its tumor microenvironment (TME) driving progression and treatment resistance.
- Current therapies inadequately address the TME's complexity, necessitating novel strategies.
- Dental pulp stem cell-derived secretome (DPSC-Sec) offers a rich source of bioactive molecules for TME modulation.
Purpose of the Study:
- To review the potential of DPSC-Sec in reprogramming the TME of oral tongue cancer.
- To explore DPSC-Sec's mechanisms of action within the TME.
- To discuss challenges and future directions for clinical translation.
Main Methods:
- Literature review of preclinical studies on DPSC-Sec and tongue cancer.
- Analysis of DPSC-Sec's molecular components and their effects on TME cells.
- Evaluation of evidence for DPSC-Sec's impact on cancer-associated fibroblasts, immune cells, extracellular matrix, and angiogenesis.
Main Results:
- DPSC-Sec demonstrates potential to inhibit cancer-associated fibroblasts and reprogram immunosuppressive cells.
- It may remodel the extracellular matrix, normalize angiogenesis, and regulate oncogenic pathways.
- Priming methods significantly influence DPSC-Sec's therapeutic potency.
Conclusions:
- DPSC-Sec is a promising therapeutic agent for modulating the tongue cancer TME.
- Further validation in immunocompetent models and rigorous safety assessments are crucial for clinical translation.
- Combination strategies with biomaterials or conventional therapies could enhance efficacy.
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