Skip to main content
Top
Published in: Cancer Cell International 1/2022

Open Access 01-12-2022 | Prostate Cancer | Primary research

SLC4A4 promotes prostate cancer progression in vivo and in vitro via AKT-mediated signalling pathway

Authors: Zelin Liu, Qinghua Wang, Guanzhong Zhai, Shuai Ke, Xi Yu, Jia Guo

Published in: Cancer Cell International | Issue 1/2022

Login to get access

Abstract

Background

Prostate cancer (PCa) is the second leading cause of cancer-related male deaths worldwide. The purpose of this study was to investigate the effects of homo sapiens solute carrier family 4 member 4 (SLC4A4), which encodes the electrogenic Na+/HCO3 cotransporter isoform 1 (NBCe1), in the development and progression of PCa.

Methods

The expression levels of SLC4A4 in PCa and normal prostate tissues were evaluated by immunohistochemistry. The SLC4A4 knockdown cell model was structured by lentiviral infection, and the knockdown efficiency was validated by RT-qPCR and Western blotting. The effects of SLC4A4 knockdown on cell proliferation, apoptosis and cycle, migration, and invasion were detected by Celigo cell counting assay and CCK-8 assay, flow cytometry analysis, wound-healing, and Transwell assay, respectively. Tumor growth in nude mice was surveyed by in vivo imaging and Ki-67 staining. Furthermore, underlying mechanism of SLC4A4 silence induced inhibition of PCa progression was explored by human phospho-kinase array.

Results

Our results revealed that SLC4A4 expression was up-regulated in PCa tissues and human PCa cell lines. High expression of SLC4A4 in tumor specimens was significantly correlated with disease progression. SLC4A4 knockdown inhibited cell proliferation, migration and invasion, while facilitated apoptosis, which was also confirmed in vivo. Moreover, SLC4A4 promoted PCa progression through the AKT-mediated signalling pathway.

Conclusion

The results of this study indicated that SLC4A4 overexpression was closely associated with the progression of PCa; SLC4A4 knockdown suppressed PCa development in vitro and in vivo. SLC4A4 acts as a tumor promotor in PCa by regulating key components of the AKT pathway and may therefore act as a potential therapeutic target for PCa treatment.
Literature
1.
go back to reference Shang Z, et al. LncRNA PCAT1 activates AKT and NF-κB signaling in castration-resistant prostate cancer by regulating the PHLPP/FKBP51/IKKα complex. Nucleic Acids Res. 2019;47(8):4211–25.PubMedPubMedCentralCrossRef Shang Z, et al. LncRNA PCAT1 activates AKT and NF-κB signaling in castration-resistant prostate cancer by regulating the PHLPP/FKBP51/IKKα complex. Nucleic Acids Res. 2019;47(8):4211–25.PubMedPubMedCentralCrossRef
3.
go back to reference Chen Z, et al. Androgen receptor-activated enhancers simultaneously regulate oncogene TMPRSS2 and lncRNA PRCAT38 in prostate cancer. Cells. 2019;8(8):864.PubMedCentralCrossRef Chen Z, et al. Androgen receptor-activated enhancers simultaneously regulate oncogene TMPRSS2 and lncRNA PRCAT38 in prostate cancer. Cells. 2019;8(8):864.PubMedCentralCrossRef
4.
6.
go back to reference Abeshouse A, Ahn J, Akbani R, Ally A, Amin S, Andry CD, Annala M, Aprikian A, Armenia J, Arora A, Auman JT. The molecular taxonomy of primary prostate cancer. Cell. 2015;163(4):1011–25.CrossRef Abeshouse A, Ahn J, Akbani R, Ally A, Amin S, Andry CD, Annala M, Aprikian A, Armenia J, Arora A, Auman JT. The molecular taxonomy of primary prostate cancer. Cell. 2015;163(4):1011–25.CrossRef
9.
go back to reference Zhou J, et al. SLC1A1, SLC16A9, and CNTN3 are potential biomarkers for the occurrence of colorectal cancer. Biomed Res Int. 2020;2020:1204605.PubMedPubMedCentral Zhou J, et al. SLC1A1, SLC16A9, and CNTN3 are potential biomarkers for the occurrence of colorectal cancer. Biomed Res Int. 2020;2020:1204605.PubMedPubMedCentral
10.
go back to reference McIntyre A, et al. Disrupting hypoxia-induced bicarbonate transport acidifies tumor cells and suppresses tumor growth. Can Res. 2016;76(13):3744–55.CrossRef McIntyre A, et al. Disrupting hypoxia-induced bicarbonate transport acidifies tumor cells and suppresses tumor growth. Can Res. 2016;76(13):3744–55.CrossRef
11.
go back to reference Xiao W, et al. MiR-223-3p promotes cell proliferation and metastasis by downregulating SLC4A4 in clear cell renal cell carcinoma. Aging. 2019;11(2):615–33.PubMedPubMedCentralCrossRef Xiao W, et al. MiR-223-3p promotes cell proliferation and metastasis by downregulating SLC4A4 in clear cell renal cell carcinoma. Aging. 2019;11(2):615–33.PubMedPubMedCentralCrossRef
12.
go back to reference Yang H, et al. Association of a novel seven-gene expression signature with the disease prognosis in colon cancer patients. Aging. 2019;11(19):8710–27.PubMedPubMedCentralCrossRef Yang H, et al. Association of a novel seven-gene expression signature with the disease prognosis in colon cancer patients. Aging. 2019;11(19):8710–27.PubMedPubMedCentralCrossRef
13.
go back to reference Gomez-Rueda H, et al. A robust biomarker of differential correlations improves the diagnosis of cytologically indeterminate thyroid cancers. Int J Mol Med. 2016;37(5):1355–62.PubMedCrossRef Gomez-Rueda H, et al. A robust biomarker of differential correlations improves the diagnosis of cytologically indeterminate thyroid cancers. Int J Mol Med. 2016;37(5):1355–62.PubMedCrossRef
14.
go back to reference Gerber JM, et al. Genome-wide comparison of the transcriptomes of highly enriched normal and chronic myeloid leukemia stem and progenitor cell populations. Oncotarget. 2013;4(5):715–28.PubMedPubMedCentralCrossRef Gerber JM, et al. Genome-wide comparison of the transcriptomes of highly enriched normal and chronic myeloid leukemia stem and progenitor cell populations. Oncotarget. 2013;4(5):715–28.PubMedPubMedCentralCrossRef
15.
go back to reference Chen X, et al. Prognostic value of SLC4A4 and its correlation with immune infiltration in colon adenocarcinoma. Medical Sci Monit Int Med J Exp Clin Res. 2020;26:e925016. Chen X, et al. Prognostic value of SLC4A4 and its correlation with immune infiltration in colon adenocarcinoma. Medical Sci Monit Int Med J Exp Clin Res. 2020;26:e925016.
16.
go back to reference Gao X, Yang J. Identification of genes related to clinicopathological characteristics and prognosis of patients with colorectal cancer. DNA Cell Biol. 2020;39(4):690–9.PubMedCrossRef Gao X, Yang J. Identification of genes related to clinicopathological characteristics and prognosis of patients with colorectal cancer. DNA Cell Biol. 2020;39(4):690–9.PubMedCrossRef
18.
go back to reference Pan Y, et al. Sensitive and visible detection of apoptotic cells on Annexin-V modified substrate using aminophenylboronic acid modified gold nanoparticles (APBA-GNPs) labeling. Biosens Bioelectron. 2014;52:62–8.PubMedCrossRef Pan Y, et al. Sensitive and visible detection of apoptotic cells on Annexin-V modified substrate using aminophenylboronic acid modified gold nanoparticles (APBA-GNPs) labeling. Biosens Bioelectron. 2014;52:62–8.PubMedCrossRef
19.
go back to reference Lim DJ, et al. Growth of an androgen-sensitive human prostate cancer cell line, LNCaP, in nude mice. Prostate. 1993;22(2):109–18.PubMedCrossRef Lim DJ, et al. Growth of an androgen-sensitive human prostate cancer cell line, LNCaP, in nude mice. Prostate. 1993;22(2):109–18.PubMedCrossRef
20.
go back to reference van Bokhoven A, et al. Molecular characterization of human prostate carcinoma cell lines. Prostate. 2003;57(3):205–25.PubMedCrossRef van Bokhoven A, et al. Molecular characterization of human prostate carcinoma cell lines. Prostate. 2003;57(3):205–25.PubMedCrossRef
21.
go back to reference Stephenson RA, et al. Metastatic model for human prostate cancer using orthotopic implantation in nude mice. J Natl Cancer Inst. 1992;84(12):951–7.PubMedCrossRef Stephenson RA, et al. Metastatic model for human prostate cancer using orthotopic implantation in nude mice. J Natl Cancer Inst. 1992;84(12):951–7.PubMedCrossRef
24.
go back to reference Uko NE, et al. Akt pathway inhibition of the solenopsin analog, 2-dodecylsulfanyl-1,-4,-5,-6-tetrahydropyrimidine. Anticancer Res. 2019;39(10):5329–38.PubMedCrossRef Uko NE, et al. Akt pathway inhibition of the solenopsin analog, 2-dodecylsulfanyl-1,-4,-5,-6-tetrahydropyrimidine. Anticancer Res. 2019;39(10):5329–38.PubMedCrossRef
25.
go back to reference Cucchiara V, et al. Genomic markers in prostate cancer decision making. Eur Urol. 2018;73(4):572–82.PubMedCrossRef Cucchiara V, et al. Genomic markers in prostate cancer decision making. Eur Urol. 2018;73(4):572–82.PubMedCrossRef
26.
go back to reference Gandhi J, et al. The molecular biology of prostate cancer: current understanding and clinical implications. Prostate Cancer Prostatic Dis. 2018;21(1):22–36.PubMedCrossRef Gandhi J, et al. The molecular biology of prostate cancer: current understanding and clinical implications. Prostate Cancer Prostatic Dis. 2018;21(1):22–36.PubMedCrossRef
27.
go back to reference Colmenares Aguilar M-G, et al. Expression of the regulated isoform of the electrogenic Na+/HCO3- cotransporter, NBCe1, is enriched in pacemaker interstitial cells of Cajal. Am J Physiol Gastrointest Liver Physiol. 2021;320(1):G93–107.PubMedCrossRef Colmenares Aguilar M-G, et al. Expression of the regulated isoform of the electrogenic Na+/HCO3- cotransporter, NBCe1, is enriched in pacemaker interstitial cells of Cajal. Am J Physiol Gastrointest Liver Physiol. 2021;320(1):G93–107.PubMedCrossRef
28.
go back to reference Parks SK, Pouyssegur J. The Na(+)/HCO3(-) Co-transporter SLC4A4 plays a role in growth and migration of colon and breast cancer cells. J Cell Physiol. 2015;230(8):1954–63.PubMedCrossRef Parks SK, Pouyssegur J. The Na(+)/HCO3(-) Co-transporter SLC4A4 plays a role in growth and migration of colon and breast cancer cells. J Cell Physiol. 2015;230(8):1954–63.PubMedCrossRef
29.
go back to reference Lee S-K, Boron WF, Parker MD. Substrate specificity of the electrogenic sodium/bicarbonate cotransporter NBCe1-A (SLC4A4, variant A) from humans and rabbits. Am J Physiol Renal Physiol. 2013;304(7):F883–99.PubMedPubMedCentralCrossRef Lee S-K, Boron WF, Parker MD. Substrate specificity of the electrogenic sodium/bicarbonate cotransporter NBCe1-A (SLC4A4, variant A) from humans and rabbits. Am J Physiol Renal Physiol. 2013;304(7):F883–99.PubMedPubMedCentralCrossRef
30.
31.
go back to reference Bellacosa A, et al. Activation of AKT kinases in cancer: implications for therapeutic targeting. Adv Cancer Res. 2005;94:29–86.PubMedCrossRef Bellacosa A, et al. Activation of AKT kinases in cancer: implications for therapeutic targeting. Adv Cancer Res. 2005;94:29–86.PubMedCrossRef
32.
go back to reference Altomare DA, Testa JR. Perturbations of the AKT signaling pathway in human cancer. Oncogene. 2005;24(50):7455–64.PubMedCrossRef Altomare DA, Testa JR. Perturbations of the AKT signaling pathway in human cancer. Oncogene. 2005;24(50):7455–64.PubMedCrossRef
33.
go back to reference Huang Y, et al. LncRNA AK023391 promotes tumorigenesis and invasion of gastric cancer through activation of the PI3K/Akt signaling pathway. J Exp Clin Cancer Res CR. 2017;36(1):194.PubMedCrossRef Huang Y, et al. LncRNA AK023391 promotes tumorigenesis and invasion of gastric cancer through activation of the PI3K/Akt signaling pathway. J Exp Clin Cancer Res CR. 2017;36(1):194.PubMedCrossRef
34.
35.
go back to reference Alzahrani AS. PI3K/Akt/mTOR inhibitors in cancer: at the bench and bedside. Semin Cancer Biol. 2019;59:125–32.PubMedCrossRef Alzahrani AS. PI3K/Akt/mTOR inhibitors in cancer: at the bench and bedside. Semin Cancer Biol. 2019;59:125–32.PubMedCrossRef
36.
go back to reference Gallardo A, et al. Increased signalling of EGFR and IGF1R, and deregulation of PTEN/PI3K/Akt pathway are related with trastuzumab resistance in HER2 breast carcinomas. Br J Cancer. 2012;106(8):1367–73.PubMedPubMedCentralCrossRef Gallardo A, et al. Increased signalling of EGFR and IGF1R, and deregulation of PTEN/PI3K/Akt pathway are related with trastuzumab resistance in HER2 breast carcinomas. Br J Cancer. 2012;106(8):1367–73.PubMedPubMedCentralCrossRef
37.
go back to reference Yu X, et al. TSPAN7 exerts anti-tumor effects in bladder cancer through the PTEN/PI3K/AKT pathway. Front Oncol. 2020;10:613869.PubMedCrossRef Yu X, et al. TSPAN7 exerts anti-tumor effects in bladder cancer through the PTEN/PI3K/AKT pathway. Front Oncol. 2020;10:613869.PubMedCrossRef
38.
39.
go back to reference Lee S-K, Boron WF. Exploring the autoinhibitory domain of the electrogenic Na+/HCO3- transporter NBCe1-B, from residues 28 to 62. J Physiol. 2018;596(16):3637–53.PubMedPubMedCentralCrossRef Lee S-K, Boron WF. Exploring the autoinhibitory domain of the electrogenic Na+/HCO3- transporter NBCe1-B, from residues 28 to 62. J Physiol. 2018;596(16):3637–53.PubMedPubMedCentralCrossRef
40.
go back to reference Paschalis A, et al. Alternative splicing in prostate cancer. Nat Rev Clin Oncol. 2018;15(11):663–75.PubMedCrossRef Paschalis A, et al. Alternative splicing in prostate cancer. Nat Rev Clin Oncol. 2018;15(11):663–75.PubMedCrossRef
41.
go back to reference Zhao J, et al. Systematic profiling of alternative splicing signature reveals prognostic predictor for prostate cancer. Cancer Sci. 2020;111(8):3020–31.PubMedPubMedCentralCrossRef Zhao J, et al. Systematic profiling of alternative splicing signature reveals prognostic predictor for prostate cancer. Cancer Sci. 2020;111(8):3020–31.PubMedPubMedCentralCrossRef
Metadata
Title
SLC4A4 promotes prostate cancer progression in vivo and in vitro via AKT-mediated signalling pathway
Authors
Zelin Liu
Qinghua Wang
Guanzhong Zhai
Shuai Ke
Xi Yu
Jia Guo
Publication date
01-12-2022
Publisher
BioMed Central
Published in
Cancer Cell International / Issue 1/2022
Electronic ISSN: 1475-2867
DOI
https://doi.org/10.1186/s12935-022-02546-6

Other articles of this Issue 1/2022

Cancer Cell International 1/2022 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine