Paclitaxel attenuates renal interstitial fibroblast activation and interstitial fibrosis by inhibiting STAT3 signaling.

Recent studies have demonstrated that paclitaxel might inhibit renal fibrosis. However, the underlying molecular mechanism remains unclear. In this study, we hypothesized that low-dose paclitaxel may block the STAT3 (signal transducer and activator of transcription 3) signaling to attenuate fibrosis in a mouse model with unilateral ureteral obstruction. Both NRK-49F cells and mice with unilateral ureteral obstruction were treated with paclitaxel. The results showed that paclitaxel treatment resulted in a dose- and time-dependent decrease in tyrosine-phosphorylated STAT3, and inhibited the expression of fibronectin, alpha-smooth muscle actin (α-SMA), and collagen I in cultured NRK-49F cells. S3I-201, an STAT3 inhibitor, also suppressed the expression of fibronectin, α-SMA, and collagen I in cultured NRK-49F cells. Mechanistically, paclitaxel treatment blocked the STAT3 activity by disrupting the association of STAT3 with tubulin and inhibiting STAT3 nucleus translocation. Furthermore, paclitaxel also ameliorated renal fibrosis by down-regulating the expression of fibronectin, α-SMA, and collagen I, and suppressed the infiltration of macrophages and production of TNF-α, IL-1β, TGF-β, and ICAM-1 (intercellular adhesion molecule 1) by inhibition of STAT3 activity in obstructive nephropathy. These results suggest that paclitaxel may block the STAT3 activity by disrupting the association of STAT3 with tubulin and inhibiting STAT3 nucleus translocation, consequently leading to the suppression of renal interstitial fibroblast activation and the development of renal fibrosis, and inhibition of proinflammatory cytokine production.

Introduction

Paclitaxel, one of the most important anticancer drugs, has been used in the treatment of different types of cancers. Recently, it has been found that paclitaxel could be promising in treating noncancer diseases.1 For example, Zhang et al2 reported that paclitaxel significantly suppressed tubulointerstitial fibrosis by inhibiting TGF-β (transforming growth factor-beta)/Smad signaling in a rat model of unilateral ureteral obstruction (UUO). Karbalay-Doust et al3 also found that paclitaxel was more effective than taurine in suppressing renal fibrosis in the UUO model. Furthermore, paclitaxel showed an antifibrosis role by blocking TGF-β/Smad/miR-192 signaling.4 However, the underlying molecular mechanism is not fully understood.

Renal interstitial fibrosis is a progressive process. The key step is the transformation of the renal fibroblasts to alpha-smooth muscle actin (α-SMA)-positive myofibroblasts in the evolution of chronic kidney disease.5,6 Signal transducer and activator of transcription 3 (STAT3) is an important member of the STAT family (STAT14, STAT5a/5b, and STAT6) and mediates cell survival and proliferation.7–9 Multiple growth factors and cytokines may activate STAT3 tyrosine phosphorylation that promotes STAT3 to form dimers and translocate to the cell nucleus to regulate the transcription of target genes.7–9 It has been reported that STAT3 activation mediates the activation of renal interstitial fibroblasts and the progression of renal fibrosis in UUO models.10,11 Interestingly, Walker et al12 reported that paclitaxel might inhibit STAT3 signaling in several tumor cell lines. In view of these findings, this study was initiated to assess whether paclitaxel can, by blocking STAT3 signaling, attenuate the activation of renal interstitial fibroblasts and the progression of renal fibrosis.

Materials and methods

Reagents and antibodies

S3I-201 was purchased from Calbiochem (La Jolla, CA, USA). Antibodies were obtained from different sources: anti-GAPDH, anti-α-SMA, anticollagen I, and antifibronectin from Santa Cruz Biotechnology (Santa Cruz, CA, USA), anti-macrophage and Gr-1 from Abcam (Cambridge, MA, USA), anti-α-tubulin from Sigma-Aldrich (St Louis, MO, USA), anti-STAT3 and anti-p-STAT3 from Cell Signaling Technology (Danvers, MA, USA). The kit for protein isolation of cytoplasm and nucleus was purchased from NobleRyde (Beijing, People’s Republic of China). All secondary antibodies were from Thermo Fisher Scientific (Waltham, MA, USA).

Cell culture and treatments

NRK-49F cells were cultured in Dulbecco’s modified Eagle’s medium (Sigma-Aldrich) supplemented with 10% fetal bovine serum, 0.5% penicillin, and streptomycin in an atmosphere of 5% CO2 and 95% air at 37°C.

Care and use of laboratory animals

Animal experiments were performed in accordance with the regulations set by the Institutional Committee for the Care and Use of Laboratory Animals of Second Xiangya Hospital, People’s Republic of China, and approved by local authorities. C57BL/6 mice were housed on a 12-hour light/dark cycle and were allowed free access to food and water.

Animal model

The UUO model was established in male C57 black mice that weighed 20–25 g (Shanghai animal center, Shanghai, People’s Republic of China), as previously described.2 Four groups of mice comprising eight animals each (total 32) were divided as follows: 1) Sham group, 2) Sham with paclitaxel (Taxol; Sigma-Aldrich) group, 3) UUO group, and 4) UUO with paclitaxel group. Paclitaxel was injected intraperitoneally at a dose of 0.3 mg/kg twice a week. The control group was administered with saline. Mice were sacrificed on day 7 after UUO or sham operation. The kidneys were harvested for various biochemical and morphological studies.

Immunoprecipitation

The immunoprecipitation was performed as previously described.12,13 Briefly, approximately 500 μg of cellular protein was immunoprecipitated with 2 μg of antibodies to STAT3 or α-tubulin for 1 hour at 4°C, followed by the addition of 15 μL of protein A/G-agarose beads (Santa Cruz Biotechnology). The precipitates were washed four times with lysis buffer and subjected to immunoblotting for p-STAT3 and STAT3.

Histology and immunohistochemistry

For the histological analysis, kidney tissues fixed with 4% buffered paraformaldehyde were embedded in paraffin and 3 μm thick sections were prepared. The sections were then stained with hematoxylin–eosin and Masson’s trichrome methods.2 The interstitial fibrosis and interstitial gross area were separately analyzed by an image analysis software of Image-Pro Plus 6 (Media Cybernetics, Inc., Bethesda, MD, USA); then we calculated the percent positive area of renal interstitial fibrosis versus renal interstitial gross area. Immunohistochemical analyses were performed using antiphospho-STAT3, anti-α-SMA, anticollagen I, antifibronectin, and antimacrophage according to the previous protocol.2,14 The total number of positive cells for p-STAT3 (as identified by nuclear staining) and macrophage in tubulointerstitium was quantified by counting the number of stained cells per field, for p-STAT3. We collected 25–30 images of a kidney from each animal at 20× magnification. Areas of positive staining for α-SMA collagen type I and fibronectin in the entire cortical tubulointerstitium (a cross section of the kidney) were examined using quantitative software of Image-Pro Plus 6 (Media Cybernetics, Inc). Briefly, the detected area of tubulointerstitium was labeled, the positive-staining parts were discriminated, and the percent positive area in the detected tubulointerstitium was then measured.2,14

Immunoblot analysis

Immunoblot was carried out as previously described.14 Briefly, cells or kidney tissues were treated with a lysis buffer (Sigma-Aldrich) containing phosphatase inhibitors (Calbiochem). Equal amounts of proteins were loaded in each well for electrophoresis using SDS–PAGE gel, followed by transferring to polyvinylidene fluoride membranes. The blots were incubated with primary antibodies overnight at 4°C and probed by the horseradish peroxidase-conjugated secondary antibodies. Bands of target and internal control protein were separately outlined, and then gray level was analyzed by an image J software (NIH, Bethesda, MD, USA); then we calculated gray ratio of target protein versus internal control protein.

Measurement of TNF-α, IL-1β, and TGF-β

The levels of TNF-α (tumor necrosis factor-α), IL-1β (interleukin-1β), and TGF-β were determined using enzyme-linked immunosorbent assay (ELISA) kits (R&D Systems Inc, Minneapolis, MN, USA) as described previously.11,13 Renal cytokine levels were normalized by the protein concentration.

Real-time polymerase chain reaction

Real-time quantitative reverse transcriptase PCR amplifications were performed in 20 μL reactions as described previously.4 The primer sets used for various genes were as follows: ICAM-1 (intercellular adhesion molecule-1): forward 5′-CTTCCAGCTACCATCCCAAA-3′, reverse 5′-CTTCAGAGGCAGGAAACAGG-3′; GADPH: forward 5′-TGCTGAGTATGTCGTGGAGTCTA-3′, reverse 5′-AGTGGGAGTTGCTGTTG AAATC-3′.

Statistical analysis

Data were calculated as mean ± SEM (standard error of the mean). One-way ANOVA, followed by the Tukey’s post hoc test, was used to compare multiple treatment groups. Two-way ANOVA was used to assess the statistical significance of the differences between multiple treatment groups at different time points. Statistical significance was set at P<0.05 or <0.01.

Results

Paclitaxel suppresses the expression of fibronectin, α-SMA, and collagen I by inhibiting STAT3 activation in cultured renal interstitial fibroblasts

Previous results have demonstrated that STAT3 mediated the activation of renal interstitial fibroblasts, characterized by the expression of fibronectin, α-SMA, and collagen I.11,15 To further investigate whether low-dose paclitaxel suppresses the activation of renal interstitial fibroblasts by inhibiting STAT3 activation, we examined the effect of paclitaxel on STAT3 activation and expression of fibronectin, α-SMA, and collagen I in NRK-49F cells. As shown in Figure 1A–D, treatment with paclitaxel resulted in a dose- and time-dependent decrease in tyrosine-phosphorylated STAT3 in NRK-49F cells. Furthermore, the expression level of fibronectin, α-SMA, and collagen I was higher in NRK-49F cells (Figure 1E and F), indicating that the cultured renal interstitial fibroblasts had the phenotypic features of myofibroblasts. Treatment with paclitaxel also significantly decreased the expression of fibronectin, α-SMA, and collagen I in a time-dependent manner. This result suggests that paclitaxel suppresses the activation of renal interstitial fibroblasts by inhibiting STAT3 activation.

Figure 1

Effect of paclitaxel on STAT3 activation and the expression of fibronectin, alpha-smooth muscle actin (α-SMA), and collagen I.

Notes: Cultured NRK-49F cells were treated with paclitaxel of the indicated concentrations for 24 hours, or exposed to 4 μM paclitaxel for the indicated time period. (A) Immunoblot analysis of p-STAT3 and STAT3 after 24 hours of treatment with 2 μM and 4 μM paclitaxel. (B) p-STAT3/STAT3 ratio was found to be activated STAT3 using gray analysis. (C) Immunoblot analysis of p-STAT3 and STAT3 after 24 and 48 hours of treatment with 4 μM paclitaxel. (D) p-STAT3/STAT3 ratio was indicated as activated STAT3 by gray analysis. (E) Immunoblot analysis of fibronectin, α-SMA, collagen I, and GAPDH after 24 and 48 hours of treatment with 4 μM paclitaxel. (F) Expression levels of fibronectin, α-SMA, and collagen I were quantified by densitometry, and normalized with GAPDH. Representative immunoblots from each group (n=8). Data are presented as mean ± SEM. Significant P-values reflecting differences are indicated over the bars (*P<0.05; **P<0.01).

Abbreviations: STAT3, signal transducer and activator of transcription 3; Taxol, paclitaxel; GAPDH, glyceraldehyde 3-phosphate dehydrogenase; SEM, standard error of the mean; α-SMA, alpha-smooth muscle actin.

Paclitaxel blocks tyrosine-phosphorylated STAT3 (Tyr705) by inhibiting the association of STAT3 with tubulin and STAT3 nucleus translocation

On the basis of the findings that STAT3 directly interacted with tubulin and that paclitaxel was a microtubule stabilization agent, we presume that paclitaxel inhibits STAT3 activation by interfering with its association with tubulin. NRK-49F cells were treated with vehicle, paclitaxel, or S3I-201, which is a novel selective inhibitor of STAT3.16 First, we confirmed that S3I-201 suppressed the expression of fibronectin, α-SMA, and collagen I by blocking STAT3 activation (Figure 2A and B). However, S3I-201 also increased the expression of p-STAT1 but did not affect that of p-STAT5 at the concentration of 50 μM (data not shown). Briefly, the cell lysate was immunoprecipitated with an anti-STAT3 antibody, followed by the immunoblot detection of STAT3 tyrosine phosphorylation (Tyr705). Both paclitaxel and S3I-201 inhibited STAT3 tyrosine phosphorylation (Tyr705) (Figure 2C and D). We further examined the effect of paclitaxel on STAT3/tubulin association by immunoprecipitation assay. The cell lysate was immunoprecipitated with an antitubulin antibody, followed by the immunoblot detection of STAT3. IgG was used as the input control. The association of STAT3 with tubulin was suppressed by paclitaxel treatment (Figure 2E and F). However, S3I-201 treatment did not affect the association between STAT3 and tubulin. Thus, paclitaxel disrupted the association of STAT3 with tubulin, independently of the effect on STAT3 phosphorylation. Because paclitaxel might inhibit the STAT3 binding to tubulin, we presume that paclitaxel might suppress STAT3 translocation. Proteins of cytoplasm and nucleus from kidneys were separately extracted using a commercial kit, followed by immunoblot. The results demonstrated that paclitaxel blocked STAT3 translocation from the cytoplasm to the nucleus (Figure 2G and H), which further supported that paclitaxel blocked STAT3 activation by inhibiting the association of STAT3 with tubulin.

Figure 2

Paclitaxel disrupts interaction of STAT3 with tubulin and inhibits STAT3 nucleus translocation.

Notes: Cultured NRK-49F cells were treated with 4 μM paclitaxel or 50 mM S3I-201 for 6 to 24 hours, followed by immunoblot for STAT3, p-STAT3, and ECM genes, and immunoprecipitation with antibodies to STAT3 or tubulin. (A) Immunoblot analysis of STAT3, p-STAT3, fibronectin, α-SMA, collagen I, and GAPDH after 24 hours of treatment with 50 mM S3I-201. (B) Expression levels of fibronectin, α-SMA, and collagen I were quantified by densitometry, and normalized with GAPDH. The density of the bands was quantitated, and p-STAT3 was normalized to STAT3 as a loading control. (C) Immunoprecipitates with antibodies to STAT3 were then subjected to immunoblot analysis of STAT3 and p-STAT3, with IgG as input control. (D) The density of the bands was quantitated, and p-STAT3 was normalized to STAT3 as a loading control. (E) Immunoprecipitates with antibodies to tubulin were then subjected to immunoblot analysis of STAT3, with IgG as input control. (F) The density of the bands was quantitated, and STAT3 was normalized to tubulin as a loading control. (G) Immunoblot analysis of STAT3 in cytoplasm and nucleus at 6 hours of treatment with paclitaxel. (H) The density of the bands was quantitated, and STAT3 was normalized to GAPDH or Lamin B as a loading control. Representative immunoblots from each group (n=8). Data are presented as mean ± SEM. Significant P-values reflecting differences are indicated over the bars (*P<0.05; **P<0.01).

Abbreviations: STAT3, signal transducer and activator of transcription 3; α-SMA, alpha-smooth muscle actin; Taxol, paclitaxel; GAPDH, glyceraldehyde 3-phosphate dehydrogenase; ECM, extracellular matrix; SEM, standard error of the mean.

Paclitaxel attenuates tubulointerstitial fibrosis in mice obstructive nephropathy

Previous results demonstrated that paclitaxel attenuated fibrosis in a rat UUO model. In this experiment, we confirmed that paclitaxel also ameliorated tubulointerstitial fibrosis and tubular injury in a mouse UUO model. Briefly, hematoxylineosin staining showed that UUO animals exhibited significant tubular atrophy on day 7, which was notably reduced with paclitaxel treatment (Figure 3A). Masson’s trichrome staining demonstrated that UUO animals exhibited marked tubulointerstitial fibrosis on day 7, which was significantly reduced by paclitaxel treatment (Figure 3B and C).

Figure 3

Paclitaxel attenuates tubulointerstitial fibrosis in a mouse UUO model.

Notes: The left ureter of male C57 mice was ligated for 7 days with or without 0.3 mg/kg paclitaxel twice a week. As a control, the Sham group was injected with saline. Kidney tissues were collected on day 7 after treatment. (A) HE-stained paraffin-embedded mouse kidney sections. (B) Representative Masson’s trichrome-stained sections. (C) Semiquantitative scores of tubulointerstitial fibrosis in the kidney cortex. Original magnifications, ×200. Representative immunoblots from each group (n=8). Data are presented as mean ± SEM. Significant P-values reflecting differences are indicated over the bars (*P<0.05; **P<0.01).

Abbreviations: UUO, unilateral ureteral obstruction; Taxol, paclitaxel; HE, hematoxylin–eosin; SEM, standard error of the mean.

Blockade of STAT3 activation is a key mechanism by which paclitaxel prevents renal fibrosis in mouse obstructive nephropathy

We have demonstrated that paclitaxel suppressed STAT3 activation in vitro. To further investigate whether paclitaxel suppresses STAT3 activation and expression of collagen I, fibronectin, and α-SMA in mouse obstructive nephropathy, we examined the effect of paclitaxel. By immunohistochemistry, we found that the expression of p-STAT3, collagen I, fibronectin, and α-SMA were markedly increased in UUO than in the Sham group on day 7, which was significantly reduced by paclitaxel treatment (Figure 4A–E). Western blot analysis indicated similar results (Figure 4F and G). These findings suggest that paclitaxel suppresses the activation of renal fibroblasts to attenuate renal fibrosis by inhibiting STAT3 activation in a mouse UUO model, being consistent with in vitro findings.

Figure 4

Paclitaxel inhibits STAT3 activation and collagen I, fibronectin, and α-SMA in a mouse UUO model.

Notes: The left ureters of male C57 mice were ligated for 7 days with or without 0.3 mg/kg paclitaxel twice a week. As a control, the Sham group was injected with saline. Kidney tissues were collected on day 7 after treatment. (A) Representative p-STAT3, collagen I, fibronectin, and α-SMA immunohistochemistry (original magnification, ×200 or ×400). (B–E) Densitometric analyses were performed for each group (n=8). (F) Immunoblot analysis of p-STAT3 and STAT3 from mice kidneys of different groups on day 7. (G) p-STAT3/STAT3 ratio was indicated as activated STAT3 using gray analysis. Representative immunoblots from each group (n=8). Data are presented as mean ± SEM. Significant P-values reflecting differences are indicated over the bars (*P<0.05; **P<0.01).

Abbreviations: STAT3, signal transducer and activator of transcription 3; α-SMA, alpha-smooth muscle actin; UUO, unilateral ureteral obstruction; Taxol, paclitaxel; SEM, standard error of the mean.

Effect of paclitaxel on macrophages and neutrophils infiltration and expression of TNF-α, IL-1β, TGF-β, and ICAM-1 in mouse obstructive nephropathy

We examined the effect of paclitaxel on macrophage and neutrophil infiltration and the expression of TNF-α, IL-1β, TGF-β, and ICAM-1. Analysis of kidney sections by immunochemistry showed a prominent interstitial infiltration of macrophages and neutrophils after obstructive injury, which was significantly reduced by paclitaxel (Figure 5A–C). The expression levels of TNF-α, IL-1β, TGF-β, and ICAM-1 were increased after obstructive injury, which were also markedly reduced by paclitaxel (Figure 6A–D). These data suggest that paclitaxel suppresses macrophage and neutrophil infiltration and proinflammatory cytokines by inhibiting STAT3 activity in UUO-induced renal fibrosis.

Figure 5

Paclitaxel inhibits infiltration of macrophages and neutrophils in a mouse UUO model.

Notes: The left ureters of male C57 mice were ligated for 7 days with or without 0.3 mg/kg paclitaxel twice a week. As a control, the Sham group was injected with saline. Kidney tissues were collected on day 7 after treatment. (A) Representative macrophage and neutrophil immunohistochemistry from kidney cortical tissues of different groups on day 7 (original magnification, ×400). (B and C) Quantitation of macrophage- and neutrophil-positive cells per total cross-sectional area was performed from each group (n=8). Data are presented as mean ± SEM. Significant P-values reflecting differences are indicated over the bars (*P<0.05; **P<0.01).

Abbreviations: UUO, unilateral ureteral obstruction; Taxol, paclitaxel; SEM, standard error of the mean.

Figure 6

Effect of paclitaxel on the expression of TNF-α, IL-1β, TGF-β, and ICAM-1.

Notes: The left ureters of male C57 mice were ligated for 7 days with or without 0.3 mg/kg paclitaxel twice a week. As a control, the Sham group was injected with saline. Kidney tissues and blood samples were collected on day 7 after treatment for determination of TNF-α (A), IL-1β (B), and TGF-β (C) by ELISA and for real-time PCR determination of ICAM-1 (D). ELISA analyses were performed for each group (n=8). Data are presented as mean ± SEM. Significant P-values reflecting differences are indicated over the bars (*P<0.05; **P<0.01).

Abbreviations: TNF-α, tumor necrosis factor-α; UUO, unilateral ureteral obstruction; Taxol, paclitaxel; IL-1β, interleukin-1β; TGF-β, transforming growth factor-beta; ICAM-1, intercellular adhesion molecule-1; ELISA, enzyme-linked immunosorbent assay; PCR, polymerase chain reaction; SEM, standard error of the mean.

Discussion and conclusion

Previous results demonstrated that paclitaxel might ameliorate renal fibrosis in a rat UUO model.2 However, the mechanism remains unclear. In this study, the results show that paclitaxel treatment inhibits the expression of α-SMA and extracellular matrix proteins in renal interstitial fibroblasts, ameliorates renal fibrosis, and suppresses the infiltration of macrophages and proinflammatory cytokines in obstructive nephropathy.

Mechanistically, we observed that paclitaxel treatment blocked the STAT3 activity in cultured renal interstitial fibroblasts and the fibrotic mouse kidney. TGF-β1, platelet-derived growth factor (PDGF), and IL-6 can induce STAT3 activation,17–20 which was detected in several human diseases associated with the development of fibrosis, including liver fibrosis, scar formation after spinal cord injury, glomerulo-nephritis, and diabetic nephropathy.9,21–25 Furthermore, Pang et al11 reported that STAT3 played an important role in mediating the activation of renal interstitial fibroblasts and the development of renal fibrosis following UUO injury. In this study, we demonstrated that paclitaxel ameliorated fibrosis by inhibiting STAT3 activity in cultured renal interstitial fibroblasts and mouse UUO models. We wanted to know how the microtubule-targeting agents inhibit STAT3 activation. Mechanistically, the interaction between STAT3 and microtubules was prevented by paclitaxel. Paclitaxel may also have an effect on nonphosphorylated forms of STAT3, thereby preventing their translocation to the nucleus. Walker et al12 demonstrated that phosphorylated STAT3 was significantly inhibited by paclitaxel at a concentration of 7 μM in MDA-MB-468, MDA-MB-231, and MCF-7 cell lines. Interestingly, paclitaxel at concentrations 2 μM or 4 μM also blocked STAT3 activation in renal interstitial fibroblasts, which indicated that different cell lines had different levels of sensitivity for paclitaxel treatment. However, paclitaxel at concentration 4 μM was a relatively high dose in most cell lines according to value of the 50% inhibitory concentration (IC50). Furthermore, paclitaxel as a chemotherapeutic agent is usually used at a dosage range from 10 to 15 mg/kg in nude mice.26,27 Consequently, paclitaxel at 0.3 mg/kg in the UUO model is lower than the dosages used in nude mice, but we found that paclitaxel at this dose also markedly inhibited p-STAT3 activation.

Inflammatory responses could accelerate the progression of renal fibrosis, in which multiple inflammatory mediators play a pivotal role.28,29 Pang et al11 reported that inhibition of STAT3 activity by S3I-201 could reduce the infiltration of neutrophils and monocytes in the obstructed kidney. In this study, we observed that the administration of paclitaxel also inhibited macrophage infiltration and the proinflammatory cytokines TNF-α, IL-1β, TGF-β, and ICAM-1. Zhang et al30 demonstrated that STAT3 activity in monocytes/macrophages was a critical mediator of macrophage migration, which supported our results. As we know, TGF-β is the major cytokine in a variety of fibrogenic processes, which initiates the transition of renal tubular epithelial cells to myofibroblasts, the cellular source for extracellular matrix synthesis.31,32 Previous results have shown that low-dose paclitaxel can significantly suppress the exacerbated TGF-β/Smad signaling in the kidney and lessen the interstitial fibrosis in the rat UUO model.2 STAT3 and Smad3 are independent signaling pathways for the regulation of fibrosis development. Ogata et al9 reported that STAT3 might directly regulate TGF-β gene expression. In our study, TGF-β expression is also reduced by paclitaxel. These results suggest that paclitaxel inhibition on inflammatory responses was another mechanism of anti-renal fibrosis.

In conclusion, our study demonstrates that paclitaxel can suppress the activation of renal fibroblasts, progression of renal fibrosis, and proinflammatory response in UUO kidney injury, suggesting a potential use of the chemotherapy drug in the treatment of renal fibrotic diseases. Mechanistically, paclitaxel treatment blocks the STAT3 activity by disrupting the association of STAT3 with tubulin and STAT3 nucleus translocation.