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The role of focal adhesion kinase in bladder cancer: translation from in vitro to ex vivo human urothelial carcinomas

Gaja Markovic

Gaja Markovic

Institute of Cell Biology, Faculty of Medicine, University of LjubljanaLjubljana, Slovenia
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Markovic, Gaja
, 
Natasa Resnik

Natasa Resnik

Institute of Cell Biology, Faculty of Medicine, University of LjubljanaLjubljana, Slovenia
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Resnik, Natasa
, 
Aleksandar Janev

Aleksandar Janev

Institute of Cell Biology, Faculty of Medicine, University of LjubljanaLjubljana, Slovenia
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Janev, Aleksandar
, 
Dasa Zupancic

Dasa Zupancic

Institute of Cell Biology, Faculty of Medicine, University of LjubljanaLjubljana, Slovenia
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Zupancic, Dasa
, 
Gasper Grubelnik

Gasper Grubelnik

Institute of Pathology, Faculty of Medicine, University of LjubljanaLjubljana, Slovenia
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Grubelnik, Gasper
, 
Marusa Debeljak

Marusa Debeljak

Clinical Institute for Special Laboratory Diagnostic, University Medical Center Ljubljana, Paediatric hospitalLjubljana, Slovenia
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Debeljak, Marusa
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Maja Cemazar

Maja Cemazar

Institute of Oncology LjubljanaLjubljana, Slovenia
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Cemazar, Maja
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Tanja Jesenko

Tanja Jesenko

Institute of Oncology LjubljanaLjubljana, Slovenia
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Jesenko, Tanja
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Masa Omerzel

Masa Omerzel

Institute of Oncology LjubljanaLjubljana, Slovenia
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Omerzel, Masa
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Tomaz Smrkolj

Tomaz Smrkolj

  • Clinical Department of Urology, University Medical Center LjubljanaLjubljana, Slovenia
  • Department of Surgery, Faculty of Medicine, University of LjubljanaLjubljana, Slovenia
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Smrkolj, Tomaz
 oraz 
Mateja Erdani Kreft

Mateja Erdani Kreft

Institute of Cell Biology, Faculty of Medicine, University of LjubljanaLjubljana, Slovenia
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Kreft, Mateja Erdani
  
05 wrz 2025
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Data publikacji: 05 wrz 2025
Zakres stron: 349 - 367
Otrzymano: 28 maj 2025
Przyjęty: 17 cze 2025
DOI: https://doi.org/10.2478/raon-2025-0052
Słowa kluczowe
© 2025 Gaja Markovic et al., published by Sciendo
This work is licensed under the Creative Commons Attribution 4.0 International License.

FIGURE 1.

Schematic representation of focal adhesion kinase (FAK) inhibition. We used in vitro models of a) the primary model of differentiated normal urothelium (diff NPU), in which normal porcine urothelial (NPU) cells were maintained in culture for 4 weeks, 3 weeks of which were in medium UroM (+Ca2+ -SFBS), b) the bladder cancer urothelium early after resection of the bladder tumour, i.e. 2-day RT4 and 2-day T24 cells (RT4 (2 d) and T24 (2 d)), and of c) the bladder cancer urothelium late after resection of the bladder tumour, i.e. 7-day RT4 and 7-day T24 cells (RT4 (7 d) and T24 (7 d)). Cells were treated with FAK inhibitors PND-1186 (1 μM and 10 μM), PF-573228 (10 μM and 100 μM) and defactinib (10 μM and 100 μM) for 2 h per day for 3 consecutive days (3 × 2 h), after which cell viability was measured.
Schematic representation of focal adhesion kinase (FAK) inhibition. We used in vitro models of a) the primary model of differentiated normal urothelium (diff NPU), in which normal porcine urothelial (NPU) cells were maintained in culture for 4 weeks, 3 weeks of which were in medium UroM (+Ca2+ -SFBS), b) the bladder cancer urothelium early after resection of the bladder tumour, i.e. 2-day RT4 and 2-day T24 cells (RT4 (2 d) and T24 (2 d)), and of c) the bladder cancer urothelium late after resection of the bladder tumour, i.e. 7-day RT4 and 7-day T24 cells (RT4 (7 d) and T24 (7 d)). Cells were treated with FAK inhibitors PND-1186 (1 μM and 10 μM), PF-573228 (10 μM and 100 μM) and defactinib (10 μM and 100 μM) for 2 h per day for 3 consecutive days (3 × 2 h), after which cell viability was measured.

FIGURE 2.

Western blot and immunohistochemistry analysis of ex vivo human bladder cancer samples. (A) Western blot analysis showing the relative expression levels of FAK, p-FAK, E-cadherin, and N-cadherin in pT1 low-grade (LG) and highgrade (HG) cancer tissues, pT2 HG cancer tissues, and the corresponding normal tissues (labelled as “normal tissue (pT1 LG)” for example), collected from the tumour-adjacent regions, which were not deemed normal at biopsy, but only after pathological evaluation. (B) Relative protein expression levels from biopsies of 2–4 patients ± the standard error of the mean (SEM) normalised to β-actin and presented as median with interquartile range. (C) Immunohistochemistry of FAK and p-FAK in normal tissue, pT1 LG and HG cancer tissues and pT2 HG cancer tissues. FAK = focal adhesion kinase; L = lumen; LP = lamina propria; U = urothelium. Scale bar: 50 μm.
Western blot and immunohistochemistry analysis of ex vivo human bladder cancer samples. (A) Western blot analysis showing the relative expression levels of FAK, p-FAK, E-cadherin, and N-cadherin in pT1 low-grade (LG) and highgrade (HG) cancer tissues, pT2 HG cancer tissues, and the corresponding normal tissues (labelled as “normal tissue (pT1 LG)” for example), collected from the tumour-adjacent regions, which were not deemed normal at biopsy, but only after pathological evaluation. (B) Relative protein expression levels from biopsies of 2–4 patients ± the standard error of the mean (SEM) normalised to β-actin and presented as median with interquartile range. (C) Immunohistochemistry of FAK and p-FAK in normal tissue, pT1 LG and HG cancer tissues and pT2 HG cancer tissues. FAK = focal adhesion kinase; L = lumen; LP = lamina propria; U = urothelium. Scale bar: 50 μm.

FIGURE 3.

Molecular characterisation of normal urothelial cells (NPU) and bladder cancer cells (RT4 and T24) in vitro.(A) Relative expression levels of UPK1B, UPK3A, CDH1, CDH2 and PTK2 were determined using qRT-PCR in differentiated NPU cells (diff NPU), 7-day RT4 and 7-day T24 cells (RT4 (7 d) and T24 (7 d)). (B) Expression of E-cadherin, N-cadherin, FAK and p-FAK in 2-day NPU cells (NPU (2 d)), diff NPU, 2-day RT4 cells (RT4 (2 d)), RT4 (7 d), 2-day T24 cells (T24 (2 d)) and T24 (7 d), determined by western blot. (C) The relative protein expression of E-cadherin, N-cadherin, FAK and p-FAK in NPU (2 d), diff NPU, RT4 (2 d), RT4 (7 d), T24 (2 d) and T24 (7 d) normalised to the expression of β-actin. The results are presented as median with interquartile range. (D) Quantification of FAK-positive RT4 (7 d) and T24 (7 d) by flow cytometry. Data are presented as the mean ± the standard error of the mean (SEM). *P < 0.05.
Molecular characterisation of normal urothelial cells (NPU) and bladder cancer cells (RT4 and T24) in vitro.(A) Relative expression levels of UPK1B, UPK3A, CDH1, CDH2 and PTK2 were determined using qRT-PCR in differentiated NPU cells (diff NPU), 7-day RT4 and 7-day T24 cells (RT4 (7 d) and T24 (7 d)). (B) Expression of E-cadherin, N-cadherin, FAK and p-FAK in 2-day NPU cells (NPU (2 d)), diff NPU, 2-day RT4 cells (RT4 (2 d)), RT4 (7 d), 2-day T24 cells (T24 (2 d)) and T24 (7 d), determined by western blot. (C) The relative protein expression of E-cadherin, N-cadherin, FAK and p-FAK in NPU (2 d), diff NPU, RT4 (2 d), RT4 (7 d), T24 (2 d) and T24 (7 d) normalised to the expression of β-actin. The results are presented as median with interquartile range. (D) Quantification of FAK-positive RT4 (7 d) and T24 (7 d) by flow cytometry. Data are presented as the mean ± the standard error of the mean (SEM). *P < 0.05.

FIGURE 4.

Effect of focal adhesion kinase (FAK) silencing on the survival of 2-day RT4 and 2-day T24 cells (RT4 (2 d) and T24 (2 d)). (A–C) Gene electrotransfer (GET) of anti-FAK plasmids p44, p45 and p46 in RT4 (2 d) did not result in statistically significant FAK silencing in RT4 cells but did result in their apoptosis. (D–F) GET of anti-FAK plasmids p44, p45 and p46 caused statistically significant FAK silencing and led to apoptosis of T24 (2 d). Plasmids p44 and p45 caused a statistically significant increase in necrosis of T24 (2 d). *P < 0.05, **P < 0.001. (G) T24 cells were stably transfected with anti-FAK plasmid p45 after 14 days. However, growth of these cells was limited to a single colony, as seen under fluorescence and phase contrast microscope. Data are presented as the mean ± the standard error of the mean (SEM).
Effect of focal adhesion kinase (FAK) silencing on the survival of 2-day RT4 and 2-day T24 cells (RT4 (2 d) and T24 (2 d)). (A–C) Gene electrotransfer (GET) of anti-FAK plasmids p44, p45 and p46 in RT4 (2 d) did not result in statistically significant FAK silencing in RT4 cells but did result in their apoptosis. (D–F) GET of anti-FAK plasmids p44, p45 and p46 caused statistically significant FAK silencing and led to apoptosis of T24 (2 d). Plasmids p44 and p45 caused a statistically significant increase in necrosis of T24 (2 d). *P < 0.05, **P < 0.001. (G) T24 cells were stably transfected with anti-FAK plasmid p45 after 14 days. However, growth of these cells was limited to a single colony, as seen under fluorescence and phase contrast microscope. Data are presented as the mean ± the standard error of the mean (SEM).

FIGURE 5.

Effect of focal adhesion kinase (FAK) inhibitors on viabilities of differentiated normal urothelial (NPU) cells (diff NPU), 2-day RT4 and 2-day T24 cells (RT4 (2 d) and T24 (2 d)). (A) Treatment with FAK inhibitor 1 μM PND-1186 for 2 h per day for 3 consecutive days (3 × 2 h) led to a significantly lower viability of T24 (2 d) than diff NPU. (B) After 3 × 2 h treatment with 100 μM PF-573228, the viability of diff NPU was significantly higher than the viabilities of RT4 (2 d) and T24 (2 d). (C) Treatment with 100 μM defactinib for 3 × 2 h resulted in the greatest decrease in the viabilities of RT4 (2 d) and T24 (2 d) compared to the viability of diff NPU. Data are presented as the mean ± the standard error of the mean (SEM). To differentiate the statistical analysis, we compare the viability between different in vitro models (*, **, ***) and the viability between the control and the treated sample within each cell type (#). #P < 0.05. *P < 0.05. **P < 0.005. ***P < 0.001.
Effect of focal adhesion kinase (FAK) inhibitors on viabilities of differentiated normal urothelial (NPU) cells (diff NPU), 2-day RT4 and 2-day T24 cells (RT4 (2 d) and T24 (2 d)). (A) Treatment with FAK inhibitor 1 μM PND-1186 for 2 h per day for 3 consecutive days (3 × 2 h) led to a significantly lower viability of T24 (2 d) than diff NPU. (B) After 3 × 2 h treatment with 100 μM PF-573228, the viability of diff NPU was significantly higher than the viabilities of RT4 (2 d) and T24 (2 d). (C) Treatment with 100 μM defactinib for 3 × 2 h resulted in the greatest decrease in the viabilities of RT4 (2 d) and T24 (2 d) compared to the viability of diff NPU. Data are presented as the mean ± the standard error of the mean (SEM). To differentiate the statistical analysis, we compare the viability between different in vitro models (*, **, ***) and the viability between the control and the treated sample within each cell type (#). #P < 0.05. *P < 0.05. **P < 0.005. ***P < 0.001.

FIGURE 6.

Effect of focal adhesion kinase (FAK) inhibitors on viabilities of differentiated normal urothelial (NPU) cells (diff NPU), 7-day RT4 and 7-day T24 cells (RT4 (7 d) and T24 (7 d)). (A) After treatment with 10 μM PND-1186 for 2 h per day for 3 consecutive days (3 × 2 h), no statistically significant differences in cell viability were observed among diff NPU, RT4 (7 d) and T24 (7 d). (B) Treatment with 100 μM PF-573228 for 3 × 2 h resulted in a significant decrease in the viabilities of both RT4 (7 d) and T24 (7 d) compared to the viability of diff NPU. (C) Treatment with 100 μM defactinib for 3 × 2 h caused the greatest difference between the viabilities of diff NPU, RT4 (7 d) and T24 (7 d). (D) Western blot of p-FAK after the 3 × 2 h treatment with 100 μM defactinib in 7-day NPU cells (NPU (7 d)), RT4 (7 d) and T24 (7 d) with GAPDH-loading control. Data are presented as the mean ± the standard error of the mean (SEM). To differentiate the statistical analysis, we compare the viability between different cell types (*, **, ***) and the viability between the control and the treated sample within each cell type (#). #P < 0.05. *P < 0.05. **P < 0.005. ***P < 0.001.
Effect of focal adhesion kinase (FAK) inhibitors on viabilities of differentiated normal urothelial (NPU) cells (diff NPU), 7-day RT4 and 7-day T24 cells (RT4 (7 d) and T24 (7 d)). (A) After treatment with 10 μM PND-1186 for 2 h per day for 3 consecutive days (3 × 2 h), no statistically significant differences in cell viability were observed among diff NPU, RT4 (7 d) and T24 (7 d). (B) Treatment with 100 μM PF-573228 for 3 × 2 h resulted in a significant decrease in the viabilities of both RT4 (7 d) and T24 (7 d) compared to the viability of diff NPU. (C) Treatment with 100 μM defactinib for 3 × 2 h caused the greatest difference between the viabilities of diff NPU, RT4 (7 d) and T24 (7 d). (D) Western blot of p-FAK after the 3 × 2 h treatment with 100 μM defactinib in 7-day NPU cells (NPU (7 d)), RT4 (7 d) and T24 (7 d) with GAPDH-loading control. Data are presented as the mean ± the standard error of the mean (SEM). To differentiate the statistical analysis, we compare the viability between different cell types (*, **, ***) and the viability between the control and the treated sample within each cell type (#). #P < 0.05. *P < 0.05. **P < 0.005. ***P < 0.001.

FIGURE 7.

Focal adhesion kinase (FAK) inhibition with 100 μM defactinib for 2 h per day for 2 consecutive days (2 × 2 h) leads to caspase-3-mediated apoptosis. (A) Treated 7-day RT4 cells (RT4 (7 d)) showed lower p-FAK-labelling than controls. White arrows indicate gaps in the distribution of actin filaments in treated RT4 cells. (B) 7-day T24 cells (T24 (7 d)) contained p-FAK labelling in clusters after treatment with 100 μM defactinib for 2 × 2 h (white arrowheads). No significant changes in actin filament localisation were observed in treated and control T24 cells. Scale bars: 50 μm (white), 10 μm (black). (C) Western blot analysis showed that cleaved caspase-3 was present only in RT4 (7 d) and T24 (7 d) after treatment with 100 μM defactinib for 2 h per day for 3 consecutive days (3 × 2 h).
Focal adhesion kinase (FAK) inhibition with 100 μM defactinib for 2 h per day for 2 consecutive days (2 × 2 h) leads to caspase-3-mediated apoptosis. (A) Treated 7-day RT4 cells (RT4 (7 d)) showed lower p-FAK-labelling than controls. White arrows indicate gaps in the distribution of actin filaments in treated RT4 cells. (B) 7-day T24 cells (T24 (7 d)) contained p-FAK labelling in clusters after treatment with 100 μM defactinib for 2 × 2 h (white arrowheads). No significant changes in actin filament localisation were observed in treated and control T24 cells. Scale bars: 50 μm (white), 10 μm (black). (C) Western blot analysis showed that cleaved caspase-3 was present only in RT4 (7 d) and T24 (7 d) after treatment with 100 μM defactinib for 2 h per day for 3 consecutive days (3 × 2 h).

The anti-focal adhesion kinase (FAK) plasmids and their respective sense pre-miRNA sequences_ Three plasmid DNA encoding different miRNA against FAK (anti-FAK plasmids) were constructed using the pcDNATM6_2-GW/EmGFP-miR plasmid backbone

Plasmid Sense pre-miRNA sequence
p44 ATCTGTTTCTGACACAGAGAC
p45 AGAAATTTCTCTCTCACGCTG
p46 ATAGCAGGCCACATGCTTTAC

List of Sus scrofa primers used for reverse transcription polymerase chain reaction (qRT-PCR)_ Primers in bold are identical as used for Homo sapiens qRT-PCR

Sus scrofa
Forward Reverse
GAPDH TGCACCACCAACTGCTTGGCA GGCATGGACCGAGGTCATGAG
HPRT1 GGACTAATTATGGACAGGACTGA CAGGTCAGCAAAGAATTTATAGC
PTK2 GCTGGATTATTTCGGTGGAG CAGTAGCCGTCGATCAGGTC
UP1B AGCCTCTACCCGCTGCTTGA GGAAGAGGTTGGGTGTGAAA
UP3A TCGTTATCACGTCCATCCTG CAGACGTGTATGAAGGCTCC
CDH1 GACGGCTTAAGCACGACTGC AACGCCTCCATTGCTTACTG
CDH2 AGTGGGATCCCCACCGCTGA ATGGAAGGCAATCCCACGTA

List of Homo sapiens primers used for reverse transcription polymerase chain reaction (qRT-PCR)_ Primers in bold are identical as used for Sus scrofa qRT-PCR

Homo sapiens
Forward Reverse
GAPDH TGCACCAACTGCTTAGC GGCATGGACTGTGGTCATGAG
HPRT1 GGACTAATTATGGACAGGACTGA CAGGTCAGCAAAGAATTTATAGC
PTK2 GGCCCAGAAGAAGGA ATGCCTTGCTTTTCGCTGT
UP1B AGCCTCTACCCACTGCTTGA GGAAGAGGTTGGGTGTGAAA
UP3A TCGTCATCACTTCCATCCTG CGGACGTGTAGGAAGACTCC
CDH1 GAGGGGTTAAGCACAACAGC AATGCCATCGTTGTTCACTG
CDH2 ACAGTGGCCACCTACAAAGG CCGAGATGGGGTTGATAATG
Język:
Angielski
Częstotliwość wydawania:
4 razy w roku
Dziedziny czasopisma:
Medycyna, Medycyna kliniczna, Medycyna wewnętrzna, Hematologia, onkologia, Radiologia
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