Adipose-derived stem cell-mediated paclitaxel delivery inhibits breast cancer growth
Open Access
- 7 September 2018
- journal article
- research article
- Published by Public Library of Science (PLoS) in PLOS ONE
- Vol. 13 (9) , e0203426
Abstract
Breast cancer represents the main malignancy in women and autologous fat grafting is a diffuse procedure in the management of post-surgical breast defects causing patients’ psychosocial problems, with high costs for the public health. Recently, beneficial effects of fat grafting during post-surgical breast reconstruction have been amplified from the enrichment with human adipose-derived stem cells (ASCs) present in the stromal vascular fraction (SVF) of adult adipose tissue isolated during intraoperatory procedures. The major concern about the ASC enrichment during post-surgery breast reconstruction depends on their potential ability to release growth factors and hormones that can promote proliferation of residual or quiescent cancer cells, with the risk of de novo cancer development or recurrence. The recent description that adult stem cells primed in vitro may be vehicle for anti-cancer drug delivery offers a new vision concerning the role of ASCs in breast reconstruction after cancer surgery. Paclitaxel (PTX) is a chemotherapeutic agent acting as a microtubule-stabilizing drug inhibiting cancer cell mitotic activity. We optimized PTX loading and release in cultured ASCs and then analyzed the effects of PTX-loaded ASCs and their conditioned medium on CG5 breast cancer survival, proliferation and apoptosis in vitro, and inCG5 xenograft in vivo. We documented that ASCs can uptake and release PTX in vitro, with slight cytotoxic effects. Interestingly, PTX-loaded ASCs in co-culture, as well as conditioned medium alone, inhibited CG5 cell proliferation and survival in vitro and xenograft tumor growth in vivo. The antitumor effect of PTX-loaded ASCs may offer a new perspective concerning the use of ASCs during breast reconstruction becoming an additional local preventive chemotherapeutic agent against tumor recurrence. However, further experiments in vitro and in vivo are needed to collect more evidence confirming the efficacy and safety in cancer patients.Keywords
This publication has 55 references indexed in Scilit:
- The FGFR1 inhibitor PD173074 induces mesenchymal–epithelial transition through the transcription factor AP-1British Journal of Cancer, 2013
- Inverse Regulation of EGFR/HER1 and HER2-4 in Normal and Malignant Human Breast TissuePLOS ONE, 2013
- Fibroblast Growth Factor Receptor 1 Activation in Mammary Tumor Cells Promotes Macrophage Recruitment in a CX3CL1-Dependent MannerPLOS ONE, 2012
- Platelet-Rich Plasma Greatly Potentiates Insulin-Induced Adipogenic Differentiation of Human Adipose-Derived Stem Cells Through a Serine/Threonine Kinase Akt-Dependent Mechanism and Promotes Clinical Fat Graft MaintenanceStem Cells Translational Medicine, 2012
- The Vascular Endothelium of the Adipose Tissue Gives Rise to Both White and Brown Fat CellsCell Metabolism, 2012
- Locoregional recurrence risk after lipofilling in breast cancer patientsAnnals of Oncology, 2011
- Safety of fat grafting in secondary breast reconstruction after cancerJournal of Plastic, Reconstructive & Aesthetic Surgery, 2011
- Regenerative Therapy and Cancer: In Vitro and In Vivo Studies of the Interaction Between Adipose-Derived Stem Cells and Breast Cancer Cells from Clinical IsolatesTissue Engineering Part A, 2011
- Regenerative Therapy After Cancer: What Are the Risks?Tissue Engineering Part B: Reviews, 2010
- Multilineage Cells from Human Adipose Tissue: Implications for Cell-Based TherapiesTissue Engineering, 2001