Your privacy, your choice

We use essential cookies to make sure the site can function. We also use optional cookies for advertising, personalisation of content, usage analysis, and social media.

By accepting optional cookies, you consent to the processing of your personal data - including transfers to third parties. Some third parties are outside of the European Economic Area, with varying standards of data protection.

See our privacy policy for more information on the use of your personal data.

for further information and to change your choices.

Skip to main content
Fig. 7 | Journal of Biomedical Science

Fig. 7

From: Decreased plasma gelsolin fosters a fibrotic tumor microenvironment and promotes chemoradiotherapy resistance in esophageal squamous cell carcinoma

Fig. 7

Overexpression of pGSN suppresses tumor growth by reducing TNC expression and CAF activation in vivo. A Tumor growth of xenografts co-transplanted with CE81T-R (EV or pGSN overexpression) and fibroblasts 3T3 cells. B and C Tumor size (B) and tumor weight (C) were measured at the end of the experiment. D ELISA analysis of circulating pGSN in mice at the end of the experiment. E, mRNA expressions of pGSN, TNC, and CAF markers (ACTA2, LIF, and TAGLN) were determined by RT-qPCR analysis. F IHC staining of pGSN, TNC, αSMA, collagen, CD86 M1 and CD206 M2 macrophage markers in tumors. Data represents mean ± s.e.m. ns: non-significant; *p < 0.05; **p < 0.01; ***p < 0.001

Back to article page