Copyright: ©Author(s) 2026.
World J Gastrointest Oncol. Jun 15, 2026; 18(6): 117697
Published online Jun 15, 2026. doi: 10.4251/wjgo.v18.i6.117697
Published online Jun 15, 2026. doi: 10.4251/wjgo.v18.i6.117697
Figure 5 In vivo anti-tumor efficacy of PTX@LP-EV in MKN45 xenograft models.
A: Schematic of the therapeutic regimen in MKN45 tumor-bearing nude mice; B: Tumor growth curves of mice treated with PBS, low-pH preconditioned macrophage-derived extracellular vesicles (LP-EV), free paclitaxel (PTX), or PTX@LP-EV; C: Final tumor weights measured at the end of the experiment; D: Representative images of immunohistochemical staining for Ki-67 and cleaved caspase-3, and TUNEL staining of tumor sections. Data in (C) represent means ± SD. Statistical significance was tested using one-way ANOVA with multiple comparison tests, dP < 0.0001. LP-EV: Low-pH preconditioned macrophage-derived extracellular vesicle; PTX: Paclitaxel.
- Citation: Wang JH, Hu ML, Shi M, Ma JL, Yang J, Wang YG. Low-pH preconditioned macrophage-derived extracellular vesicles enable targeted and enhanced paclitaxel therapy in gastric cancer. World J Gastrointest Oncol 2026; 18(6): 117697
- URL: https://www.wjgnet.com/1948-5204/full/v18/i6/117697.htm
- DOI: https://dx.doi.org/10.4251/wjgo.v18.i6.117697