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COMPARISON OF THE EFFECTS OF DOCETAXEL and AMYGDALIN TREATMENT ON CELL DEATH, INTEGRIN-α and INTEGRIN-β EXPRESSIONS IN DU145 PROSTATE CANCER CELL LINE

Year 2024, Volume: 25 Issue: 4, 420 - 428, 21.10.2024
https://doi.org/10.18229/kocatepetip.1402118

Abstract

OBJECTIVE: Prostate cancer (PC) ranks second among cancer-related deaths in men, and most deaths are caused by metastasis. Integrins, which are cell surface receptors, play an important role in cancer metastasis. It has been shown that integrin alpha2beta1 expression is effective in cell adhesion, migration, and invasion by increasing binding to collagen I in metastatic PCs. Docetaxel chemotherapy is used in PC, but it is ineffective in advanced stages. Amygdalin is a cyanogenic glycoside commonly found in fruit seeds, there is conflict in the literature regarding its effectiveness in cancer treatment. We aimed to compare the effects of Amygdalin and Docetaxel treatments on the DU145 prostate cancer cell line on integrinalfa2 (ITGA2) and integrinbeta1 (ITGB1) expressions, as well as their effects on cell death, Caspase-3, and Beclin-1.
MATERIAL AND METHODS: Propagated DU145 cells were divided into four groups. Amygdalin was given to the first group, Docetaxel was given to the second group, and Amygdalin andDocetaxel were given together to the third group. They were exposed to the active substances for 24 hours. The fourth group (Control) was not given any substance. mRNA levels of ITGA2 and ITGB1 genes were determined by the Real-time PCR method. Caspase-3 and Beclin-1 staining were performed immunocytochemically to evaluate cell death.
RESULTS: There was an increase in ITGA2 and ITGB1 expressions in the groups administered by Amygdalin and by Docetaxel (P<0.05). The decrease in ITGB1 expression was significant in the group given Amygdalin+Docetaxel (P<0.001). Caspase-3 (P<0.05) and Beclin-1 (P<0.05) immunoreactivities were observed to increase in all three groups compared to the control group.
CONCLUSIONS: It was observed that Docetaxel increased cell death more than Amygdalin in DU145 PC cells, and when Amygdalin and Docetaxel were used together, ITGA2 and ITGB1 expressions were significantly reduced. Our results suggest that dual treatment of Amygdalin and Docetaxel may prevent prostate cancer metastases.

Project Number

19.TIP.013

References

  • 1. Sung H, Ferlay JS, Rebecca L, et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA: a cancer journal for clinicians, 2021;71(3):209-49.
  • 2. Reiter R, Kernion JD. Epidemiology, etiology, and prevention of prostate cancer. Campbell’s urology, 2002;4:2489-95.
  • 3. Swami U, McFarland TR, Nussenzveig R, Agarwal N. Advanced prostate cancer: treatment advances and future directions. Trends in Cancer. 2020;6(8):702-15.
  • 4. Boettcher AN, Osman A, Morgans A, et al. Past, current, and future of immunotherapies for prostate cancer. Frontiers in oncology. 2019;9:884.
  • 5. Bubendorf L, Schöpfer A, Wagner U, Sauther G, Moch H, Willi N. Metastatic patterns of prostate cancer: an autopsy study of 1,589 patients. Human Pathology. 2000;31(5):578-83.
  • 6. Mottet N, Belmunt J, Bolla M, et al. EAU guidelines on prostate cancer. Part II: Treatment of advanced, relapsing, and castration-resistant prostate cancer. Actas Urológicas Españolas (English Edition). 2011:35(10):565-79.
  • 7. Cornford P, Bergh RCN, Briers E, et al. EAU-EANM-ESTRO-ESUR-SIOG guidelines on prostate cancer. Part II— 2020 update: treatment of relapsing and metastatic prostate cancer. European Urology. 2021:79(2):263-82.
  • 8. Litwin MS, Tan HJ. The diagnosis and treatment of prostate cancer: a review. Jama. 2017;317(24):2532-42.
  • 9. Weiner AB, Kundu SD. A Contemporary Approach to Treatment and Outcomes. Urology, an Issue of Medical Clinics of North America. E-Book. 2018:102(2):215-29.
  • 10. Gaupel AC, Wang WW, Mordan-McCombs S, Lee ECY, Tenniswood M. Xenograft, Transgenic, and Knockout Models of Prostate Cancer, in Animal Models for the study of Human Disease. Elsevier. 2013;973-95.
  • 11. Nader R, El Amm J, Aragon-Ching JB. Role of chemotherapy in prostate cancer. Asian Journal of Andrology. 2018;20(3):221-29.
  • 12. Süer E, Hamidi N, Gökçe İ, Baltacı S. The Eficiency of Docetaxel Chemotherapy on Castration Resistant Prostate Cancer: Singe Center Experience. Bulletin of Urooncology. 2017;16(3):77-81.
  • 13. Avcı ÇB, Usluer Y, Şıvga D, Söğütlü F, Dündar M, Gündüz C. Rapamisinin prostat kanseri hücre hatlarındaki etkisi. Ege Tıp Dergisi. 2013;52(1):7-14.
  • 14. Wallis CJ, Klaassen Z, Bhindi B, et al. Comparison of abiraterone acetate and docetaxel with androgen deprivation therapy in high-risk and metastatic hormone-naive prostate cancer: a systematic review and network meta-analysis. European Urology. 2018:73(6):834-44.
  • 15. Tsakalozou E, Eckman AM, Bae Y. Combination effects of docetaxel and doxorubicin in hormone-refractory prostate cancer cells. Biochemistry research international. 2012; 2012:1-10.
  • 16. Song Z, Xu X. Advanced research on anti-tumor effects of amygdalin. Journal of cancer research and therapeutics. 2014:10(5):3-7.
  • 17. Chen Y, Ma J, Wang F. Amygdalin induces apoptosis in human cervical cancer cell line HeLa cells. Immunopharmacology and immunotoxicology. 2013;35(1):43-51.
  • 18. Park H-J, Yoon S, Han L, et al. Amygdalin inhibits genes related to cell cycle in SNU-C4 human colon cancer cells. World Journal of Gastroenterology. 2005;11(33):5156.
  • 19. Chang H-K, Shin M, Yang H, et al. Amygdalin induces apoptosis through regulation of Bax and Bcl-2 expressions in human DU145 and LNCaP prostate cancer cells. Biological and Pharmaceutical Bulletin. 2006;29(8):1597-602.
  • 20. Makarević J, Tsaur I, Juengel E, et al. Amygdalin delays cell cycle progression and blocks growth of prostate Cancer Cells in Vitro. Life Sciences. 2016:147:137-42.
  • 21. Hynes RO. Integrins: versatility, modulation, and signaling in cell adhesion. Cell. 1992; 69(1):11-25.
  • 22. Eke I, Cordes N. Focal adhesion signaling and therapy resistance in cancer. in Seminars in Cancer Biology. Elsevier. 2015:31:65-75.
  • 23. Seguin L, Desgrosellier JS, Weis SM, Cheresh DA. Integrins and cancer: regulators of cancer stemness, metastasis, and drug resistance. Trends in Cell Biology. 2015; 25(4):234-240.
  • 24. Westendorf JJ, Hoeppner L. Type I collagen receptor ({alpha} 2 {beta} 1) signaling promotes the growth of human prostate cancer cells within the bone: Hall CL, Dai J, van Golen KL, Keller ET, Long MW, Departments of Urology and Internal Medicine, University of Michigan, MI. in Urologic Oncology: Seminars and Original Investigations. 2007;25(2):179-80.
  • 25. Hoogland AM, Verhoef E, Roobol M, et al. Validation of stem cell markers in clinical prostate cancer: α6‐ Integrin is predictive for non‐aggressive disease. The Prostate. 2014;74(5):488-96.
  • 26. Adorno-Cruz V, Liu H. Regulation and functions of integrin α2 in cell adhesion and disease. Genes & diseases. 2019;6(1):16-24.
  • 27. Salemi Z, Azizi R, Fallahian F, Aghaei M. Integrin α2β1 inhibition attenuates prostate cancer cell proliferation by cell cycle arrest, promoting apoptosis and reducing epithelial-mesenchymal transition. J Cell Physiol. 2021:236(7):4954-65.
  • 28. Cristofani R, Marelli M, Cicardi M, et al. Dual role of autophagy on docetaxel-sensitivity in prostate cancer cells. Cell Death Disease. 2018;9:889.
  • 29. Pfaffl MW, Horgan GW, Dempfle L. Relative expression software tool (REST©) for group-wise comparison and statistical analysis of relative expression results in real-time PCR. Nucleic acids research. 2002;30(9):36.
  • 30. Mazières J, Brugger W, Cappuzzo F, et al. Evaluation of EGFR protein expression by immunohistochemistry using H-score and the magnification rule: Re-analysis of the SATURN study. Lung Cancer. 2013;82(2):231-237.
  • 31. Heidenreich A, Bastian PJ, Belmunt J, et al. EAU guidelines on prostate cancer. Part 1: screening, diagnosis, and treatment of clinically localised disease. European Urology. 2011;59(1):61-71.
  • 32. Sottnik JL, Daignault-Newton S, Morissey C, Hussain M, Keller E, Hall C. Integrin alpha 2 beta 1 (α 2 β 1) promotes prostate cancer skeletal metastasis. Clinical & experimental metastasis. 2013;30(5):569-78.
  • 33. Ojalill M, Parikainen M, Rappu P, et al. Integrin α2β1 decelerates proliferation, but promotes survival and invasion of prostate cancer cells. Oncotarget. 2018:9(65):32435.
  • 34. Liu C, Zhu Y, Lou W, et al. Functional p53 determines docetaxel sensitivity in prostate cancer cells. The Prostate. 2013;73(4):418-27.
  • 35. Budman DR, Calabro A, Kreis W. Synergistic and antagonistic combinations of drugs in human prostate cancer cell lines in vitro. Anti-Cancer Drugs. 2002;13(10):1011-6.
  • 36. Holland JC. Why patients seek unproven cancer remedies: a psychological perspective. CA Cancer J Clin. 1982;32(1):10-40.
  • 37. Newmark J, Brady RO, Grimley PM, Thistlethwaite JR. Amygdalin (Laetrile) and prunasin beta- glucosidases: distribution in germ-free rat and in human tumor tissue. Proceedings of the National Academy of Sciences. 1981;78(10):6513-6.
  • 38. Moertel CG, Fleming TR, Rubin J, et al. A clinical trial of amygdalin (Laetrile) in the treatment of human cancer. New England Journal of Medicine. 1982;306(4):201-6.
  • 39. Bitting TH. Drugs--Federal Drug Administration ban on Laetrile treatments for terminally ill cancer patients is arbitrary and capricious. Tulsa Law J. 1978;14:222-5.
  • 40. Blaheta RA, Nelson K, Haferkamp A, Juengel E. Amygdalin, quackery or cure? Phytomedicine. 2016;23(4):367-76.
  • 41. Mani J, Neuschafer J, Resch C, et al. Amygdalin Modulates Prostate Cancer Cell Adhesion and Migration In Vitro. Nutr Cancer. 2020;72(3):528-37.
  • 42. Tsaur I, Tomas A, Monecke M, et al. Amygdalin Exerts Antitumor Activity in Taxane-Resistant Prostate Cancer Cells. Cancers (Basel). 2022;14(13):3111.
  • 43. Kostenuik PJ, Sanchez-Sweatman O, Orr FW, Singh G. Bone cell matrix promotes the adhesion of human prostatic carcinoma cells via the α2β1 integrin. Clinical & Experimental Metastasis. 1996;14(1):19-26.
  • 44. Lang SH, Clarke NW, George NJR, Testa NG. Primary prostatic epithelial cell binding to human bone marrow stroma and the role of a2b1 integrin. Clinical & Experimental Metastasis. 1997;15(3):218-27.
  • 45. Collins AT, Habib FK, Maitland NJ, Neal DE. Identification and isolation of human prostate epithelial stem cells based on α2β1-integrin expression. Journal of cell science. 2001;114(21):3865-72.
  • 46. Bonkhoff H, Stein U, Remberger K. Differential expression of α6 and α2 very late antigen integrins in the normal, hyperplastic, and neoplastic prostate: simultaneous demonstration of cell surface receptors and their extracellular ligands. Human pathology. 1993;24(3):243-8.
  • 47. Goldstein AS, Lawson DA, Cheng D, Owen N. Trop2 identifies a subpopulation of murine and human prostate basal cells with stem cell characteristics. Proceedings of the National Academy of Sciences. 2008;105(52):20882-7.
  • 48. Koistinen P, Heino J. Integrins in cancer cell invasion, in Madame Curie Bioscience Database. 2013. Landes Bioscience https://www.ncbi.nlm.nih.gov/books/NBK6070/, Erişim tarihi:05.12.2023.
  • 49. Festuccia C, Bologna M, Gravina GL, et al. Osteoblast conditioned media contain TGF‐β1 and modulate the migration of prostate tumor cells and their interactions with extracellular matrix components. International Journal of Cancer. 1999;81(3):395-403.

DU145 PROSTAT KANSERİ HÜCRE HATTINDA DOSETAKSEL ve AMİGDALİN TEDAVİSİNİN HÜCRE ÖLÜMÜ, İNTEGRİN-α ve İNTEGRİN-β EKSPRESYONLARI ÜZERİNDEN ETKİLERİNİN KARŞILAŞTIRILMASI

Year 2024, Volume: 25 Issue: 4, 420 - 428, 21.10.2024
https://doi.org/10.18229/kocatepetip.1402118

Abstract

AMAÇ: Prostat kanseri (PK) erkeklerde kansere bağlı ölümler arasında ikinci sırada yer almaktadır ve ölümlerin çoğu metastaz kaynaklıdır. Kanser metastazında hücre yüzey reseptörleri olan integrinler önemli rol oynarlar. İntegrin alfa2beta1’in metastatik prostat kanserlerinde kollajen I’e bağlanmayı artırarak hücre adezyon, migrasyon ve invazyonunda etkili olduğu gösterilmiştir. Prostat kanserinde Dosetaksel kemoterapisi kullanılmakta fakat ileri evrelerde bu tedavi etkisiz kalmaktadır. Amigdalin meyve tohumlarında yaygın olarak bulunan siyanojenik bir glikozittir ve kanser tedavisinde kullanımı konusunda literatürde çelişkiler bulunmaktadır. Çalışmamızda Amigdalin ve Dosetaksel tedavilerinin DU145 prostat kanseri hücre hattına olan etkilerini integrinalfa2 (ITGA2) ve integrinbeta1 (ITGB1) ekspresyonları, ayrıca hücre ölümü üzerine olan etkilerini Caspase-3 ve Beclin-1 üzerinden karşılaştırmayı amaçladık.
GEREÇ VE YÖNTEM: DU145 hücreleri çoğaltılarak dört gruba ayrıldı. Birinci gruba Amygdalin, ikinci gruba Dosetaksel, üçüncü gruba Amygdalin ve Dosetaksel birlikte verilerek 24 saat boyunca aktif maddelere maruz bırakıldı. Dördüncü gruba (Kontrol) herhangi bir madde verilmedi. ITGA2 ve ITGB1 genlerinin mRNA düzeyleri Real-Time PCR yöntemiyle belirlendi. Hücre ölümünü değerlendirmek için immünositokimyasal olarak Caspase-3 ve Beclin-1 boyamaları yapıldı.
BULGULAR: Amigdalin, Dosetaksel uygulanan gruplarda ITGA2 ve ITGB1 ekspresyonlarında artış görüldü (P<0.05). Amigdalin+Dosetaksel verilen grupta ITGB1 ekspresyonundaki azalma anlamlıydı (P<0,001). Caspase-3 (P<0.05) ve Beclin-1 (P<0.05) immünoreaktivitelerinin her üç grupta kontrol grubuna kıyasla arttığı gözlendi.
SONUÇ: DU145 PK hücrelerinde Dosetaksel’in hücre ölümünü Amigdaline göre daha çok artırdığı, Amigdalin ve dosetakselin birlikte kullanıldığında ITGA2 ve ITGB1 ekspresyonlarını önemli şekilde azalttığı gözlemlenmiştir. Sonuçlarımız Amigdalin ve dosetakselin ikili tedavisinin prostat kanseri metastazlarının önüne geçebileceğini düşündürmektedir.

Supporting Institution

Afyonkarahisar Health Science University Scientific Research Projects Coordination Unit

Project Number

19.TIP.013

References

  • 1. Sung H, Ferlay JS, Rebecca L, et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA: a cancer journal for clinicians, 2021;71(3):209-49.
  • 2. Reiter R, Kernion JD. Epidemiology, etiology, and prevention of prostate cancer. Campbell’s urology, 2002;4:2489-95.
  • 3. Swami U, McFarland TR, Nussenzveig R, Agarwal N. Advanced prostate cancer: treatment advances and future directions. Trends in Cancer. 2020;6(8):702-15.
  • 4. Boettcher AN, Osman A, Morgans A, et al. Past, current, and future of immunotherapies for prostate cancer. Frontiers in oncology. 2019;9:884.
  • 5. Bubendorf L, Schöpfer A, Wagner U, Sauther G, Moch H, Willi N. Metastatic patterns of prostate cancer: an autopsy study of 1,589 patients. Human Pathology. 2000;31(5):578-83.
  • 6. Mottet N, Belmunt J, Bolla M, et al. EAU guidelines on prostate cancer. Part II: Treatment of advanced, relapsing, and castration-resistant prostate cancer. Actas Urológicas Españolas (English Edition). 2011:35(10):565-79.
  • 7. Cornford P, Bergh RCN, Briers E, et al. EAU-EANM-ESTRO-ESUR-SIOG guidelines on prostate cancer. Part II— 2020 update: treatment of relapsing and metastatic prostate cancer. European Urology. 2021:79(2):263-82.
  • 8. Litwin MS, Tan HJ. The diagnosis and treatment of prostate cancer: a review. Jama. 2017;317(24):2532-42.
  • 9. Weiner AB, Kundu SD. A Contemporary Approach to Treatment and Outcomes. Urology, an Issue of Medical Clinics of North America. E-Book. 2018:102(2):215-29.
  • 10. Gaupel AC, Wang WW, Mordan-McCombs S, Lee ECY, Tenniswood M. Xenograft, Transgenic, and Knockout Models of Prostate Cancer, in Animal Models for the study of Human Disease. Elsevier. 2013;973-95.
  • 11. Nader R, El Amm J, Aragon-Ching JB. Role of chemotherapy in prostate cancer. Asian Journal of Andrology. 2018;20(3):221-29.
  • 12. Süer E, Hamidi N, Gökçe İ, Baltacı S. The Eficiency of Docetaxel Chemotherapy on Castration Resistant Prostate Cancer: Singe Center Experience. Bulletin of Urooncology. 2017;16(3):77-81.
  • 13. Avcı ÇB, Usluer Y, Şıvga D, Söğütlü F, Dündar M, Gündüz C. Rapamisinin prostat kanseri hücre hatlarındaki etkisi. Ege Tıp Dergisi. 2013;52(1):7-14.
  • 14. Wallis CJ, Klaassen Z, Bhindi B, et al. Comparison of abiraterone acetate and docetaxel with androgen deprivation therapy in high-risk and metastatic hormone-naive prostate cancer: a systematic review and network meta-analysis. European Urology. 2018:73(6):834-44.
  • 15. Tsakalozou E, Eckman AM, Bae Y. Combination effects of docetaxel and doxorubicin in hormone-refractory prostate cancer cells. Biochemistry research international. 2012; 2012:1-10.
  • 16. Song Z, Xu X. Advanced research on anti-tumor effects of amygdalin. Journal of cancer research and therapeutics. 2014:10(5):3-7.
  • 17. Chen Y, Ma J, Wang F. Amygdalin induces apoptosis in human cervical cancer cell line HeLa cells. Immunopharmacology and immunotoxicology. 2013;35(1):43-51.
  • 18. Park H-J, Yoon S, Han L, et al. Amygdalin inhibits genes related to cell cycle in SNU-C4 human colon cancer cells. World Journal of Gastroenterology. 2005;11(33):5156.
  • 19. Chang H-K, Shin M, Yang H, et al. Amygdalin induces apoptosis through regulation of Bax and Bcl-2 expressions in human DU145 and LNCaP prostate cancer cells. Biological and Pharmaceutical Bulletin. 2006;29(8):1597-602.
  • 20. Makarević J, Tsaur I, Juengel E, et al. Amygdalin delays cell cycle progression and blocks growth of prostate Cancer Cells in Vitro. Life Sciences. 2016:147:137-42.
  • 21. Hynes RO. Integrins: versatility, modulation, and signaling in cell adhesion. Cell. 1992; 69(1):11-25.
  • 22. Eke I, Cordes N. Focal adhesion signaling and therapy resistance in cancer. in Seminars in Cancer Biology. Elsevier. 2015:31:65-75.
  • 23. Seguin L, Desgrosellier JS, Weis SM, Cheresh DA. Integrins and cancer: regulators of cancer stemness, metastasis, and drug resistance. Trends in Cell Biology. 2015; 25(4):234-240.
  • 24. Westendorf JJ, Hoeppner L. Type I collagen receptor ({alpha} 2 {beta} 1) signaling promotes the growth of human prostate cancer cells within the bone: Hall CL, Dai J, van Golen KL, Keller ET, Long MW, Departments of Urology and Internal Medicine, University of Michigan, MI. in Urologic Oncology: Seminars and Original Investigations. 2007;25(2):179-80.
  • 25. Hoogland AM, Verhoef E, Roobol M, et al. Validation of stem cell markers in clinical prostate cancer: α6‐ Integrin is predictive for non‐aggressive disease. The Prostate. 2014;74(5):488-96.
  • 26. Adorno-Cruz V, Liu H. Regulation and functions of integrin α2 in cell adhesion and disease. Genes & diseases. 2019;6(1):16-24.
  • 27. Salemi Z, Azizi R, Fallahian F, Aghaei M. Integrin α2β1 inhibition attenuates prostate cancer cell proliferation by cell cycle arrest, promoting apoptosis and reducing epithelial-mesenchymal transition. J Cell Physiol. 2021:236(7):4954-65.
  • 28. Cristofani R, Marelli M, Cicardi M, et al. Dual role of autophagy on docetaxel-sensitivity in prostate cancer cells. Cell Death Disease. 2018;9:889.
  • 29. Pfaffl MW, Horgan GW, Dempfle L. Relative expression software tool (REST©) for group-wise comparison and statistical analysis of relative expression results in real-time PCR. Nucleic acids research. 2002;30(9):36.
  • 30. Mazières J, Brugger W, Cappuzzo F, et al. Evaluation of EGFR protein expression by immunohistochemistry using H-score and the magnification rule: Re-analysis of the SATURN study. Lung Cancer. 2013;82(2):231-237.
  • 31. Heidenreich A, Bastian PJ, Belmunt J, et al. EAU guidelines on prostate cancer. Part 1: screening, diagnosis, and treatment of clinically localised disease. European Urology. 2011;59(1):61-71.
  • 32. Sottnik JL, Daignault-Newton S, Morissey C, Hussain M, Keller E, Hall C. Integrin alpha 2 beta 1 (α 2 β 1) promotes prostate cancer skeletal metastasis. Clinical & experimental metastasis. 2013;30(5):569-78.
  • 33. Ojalill M, Parikainen M, Rappu P, et al. Integrin α2β1 decelerates proliferation, but promotes survival and invasion of prostate cancer cells. Oncotarget. 2018:9(65):32435.
  • 34. Liu C, Zhu Y, Lou W, et al. Functional p53 determines docetaxel sensitivity in prostate cancer cells. The Prostate. 2013;73(4):418-27.
  • 35. Budman DR, Calabro A, Kreis W. Synergistic and antagonistic combinations of drugs in human prostate cancer cell lines in vitro. Anti-Cancer Drugs. 2002;13(10):1011-6.
  • 36. Holland JC. Why patients seek unproven cancer remedies: a psychological perspective. CA Cancer J Clin. 1982;32(1):10-40.
  • 37. Newmark J, Brady RO, Grimley PM, Thistlethwaite JR. Amygdalin (Laetrile) and prunasin beta- glucosidases: distribution in germ-free rat and in human tumor tissue. Proceedings of the National Academy of Sciences. 1981;78(10):6513-6.
  • 38. Moertel CG, Fleming TR, Rubin J, et al. A clinical trial of amygdalin (Laetrile) in the treatment of human cancer. New England Journal of Medicine. 1982;306(4):201-6.
  • 39. Bitting TH. Drugs--Federal Drug Administration ban on Laetrile treatments for terminally ill cancer patients is arbitrary and capricious. Tulsa Law J. 1978;14:222-5.
  • 40. Blaheta RA, Nelson K, Haferkamp A, Juengel E. Amygdalin, quackery or cure? Phytomedicine. 2016;23(4):367-76.
  • 41. Mani J, Neuschafer J, Resch C, et al. Amygdalin Modulates Prostate Cancer Cell Adhesion and Migration In Vitro. Nutr Cancer. 2020;72(3):528-37.
  • 42. Tsaur I, Tomas A, Monecke M, et al. Amygdalin Exerts Antitumor Activity in Taxane-Resistant Prostate Cancer Cells. Cancers (Basel). 2022;14(13):3111.
  • 43. Kostenuik PJ, Sanchez-Sweatman O, Orr FW, Singh G. Bone cell matrix promotes the adhesion of human prostatic carcinoma cells via the α2β1 integrin. Clinical & Experimental Metastasis. 1996;14(1):19-26.
  • 44. Lang SH, Clarke NW, George NJR, Testa NG. Primary prostatic epithelial cell binding to human bone marrow stroma and the role of a2b1 integrin. Clinical & Experimental Metastasis. 1997;15(3):218-27.
  • 45. Collins AT, Habib FK, Maitland NJ, Neal DE. Identification and isolation of human prostate epithelial stem cells based on α2β1-integrin expression. Journal of cell science. 2001;114(21):3865-72.
  • 46. Bonkhoff H, Stein U, Remberger K. Differential expression of α6 and α2 very late antigen integrins in the normal, hyperplastic, and neoplastic prostate: simultaneous demonstration of cell surface receptors and their extracellular ligands. Human pathology. 1993;24(3):243-8.
  • 47. Goldstein AS, Lawson DA, Cheng D, Owen N. Trop2 identifies a subpopulation of murine and human prostate basal cells with stem cell characteristics. Proceedings of the National Academy of Sciences. 2008;105(52):20882-7.
  • 48. Koistinen P, Heino J. Integrins in cancer cell invasion, in Madame Curie Bioscience Database. 2013. Landes Bioscience https://www.ncbi.nlm.nih.gov/books/NBK6070/, Erişim tarihi:05.12.2023.
  • 49. Festuccia C, Bologna M, Gravina GL, et al. Osteoblast conditioned media contain TGF‐β1 and modulate the migration of prostate tumor cells and their interactions with extracellular matrix components. International Journal of Cancer. 1999;81(3):395-403.
There are 49 citations in total.

Details

Primary Language English
Subjects Cell Development, Proliferation and Death, Receptors and Membrane Biology, Cancer Cell Biology, Cancer Therapy (Excl. Chemotherapy and Radiation Therapy)
Journal Section Articles
Authors

Çiğdem Karaca 0000-0003-2106-2422

Evrim Suna Arıkan Söylemez 0000-0002-8550-793X

Esra Aslan 0000-0002-3191-4978

Fatma Fırat 0000-0003-0027-5138

Zafer Söylemez 0000-0002-0415-8118

Project Number 19.TIP.013
Publication Date October 21, 2024
Submission Date December 10, 2023
Acceptance Date April 20, 2024
Published in Issue Year 2024 Volume: 25 Issue: 4

Cite

APA Karaca, Ç., Arıkan Söylemez, E. S., Aslan, E., Fırat, F., et al. (2024). COMPARISON OF THE EFFECTS OF DOCETAXEL and AMYGDALIN TREATMENT ON CELL DEATH, INTEGRIN-α and INTEGRIN-β EXPRESSIONS IN DU145 PROSTATE CANCER CELL LINE. Kocatepe Tıp Dergisi, 25(4), 420-428. https://doi.org/10.18229/kocatepetip.1402118
AMA Karaca Ç, Arıkan Söylemez ES, Aslan E, Fırat F, Söylemez Z. COMPARISON OF THE EFFECTS OF DOCETAXEL and AMYGDALIN TREATMENT ON CELL DEATH, INTEGRIN-α and INTEGRIN-β EXPRESSIONS IN DU145 PROSTATE CANCER CELL LINE. KTD. October 2024;25(4):420-428. doi:10.18229/kocatepetip.1402118
Chicago Karaca, Çiğdem, Evrim Suna Arıkan Söylemez, Esra Aslan, Fatma Fırat, and Zafer Söylemez. “COMPARISON OF THE EFFECTS OF DOCETAXEL and AMYGDALIN TREATMENT ON CELL DEATH, INTEGRIN-α and INTEGRIN-β EXPRESSIONS IN DU145 PROSTATE CANCER CELL LINE”. Kocatepe Tıp Dergisi 25, no. 4 (October 2024): 420-28. https://doi.org/10.18229/kocatepetip.1402118.
EndNote Karaca Ç, Arıkan Söylemez ES, Aslan E, Fırat F, Söylemez Z (October 1, 2024) COMPARISON OF THE EFFECTS OF DOCETAXEL and AMYGDALIN TREATMENT ON CELL DEATH, INTEGRIN-α and INTEGRIN-β EXPRESSIONS IN DU145 PROSTATE CANCER CELL LINE. Kocatepe Tıp Dergisi 25 4 420–428.
IEEE Ç. Karaca, E. S. Arıkan Söylemez, E. Aslan, F. Fırat, and Z. Söylemez, “COMPARISON OF THE EFFECTS OF DOCETAXEL and AMYGDALIN TREATMENT ON CELL DEATH, INTEGRIN-α and INTEGRIN-β EXPRESSIONS IN DU145 PROSTATE CANCER CELL LINE”, KTD, vol. 25, no. 4, pp. 420–428, 2024, doi: 10.18229/kocatepetip.1402118.
ISNAD Karaca, Çiğdem et al. “COMPARISON OF THE EFFECTS OF DOCETAXEL and AMYGDALIN TREATMENT ON CELL DEATH, INTEGRIN-α and INTEGRIN-β EXPRESSIONS IN DU145 PROSTATE CANCER CELL LINE”. Kocatepe Tıp Dergisi 25/4 (October 2024), 420-428. https://doi.org/10.18229/kocatepetip.1402118.
JAMA Karaca Ç, Arıkan Söylemez ES, Aslan E, Fırat F, Söylemez Z. COMPARISON OF THE EFFECTS OF DOCETAXEL and AMYGDALIN TREATMENT ON CELL DEATH, INTEGRIN-α and INTEGRIN-β EXPRESSIONS IN DU145 PROSTATE CANCER CELL LINE. KTD. 2024;25:420–428.
MLA Karaca, Çiğdem et al. “COMPARISON OF THE EFFECTS OF DOCETAXEL and AMYGDALIN TREATMENT ON CELL DEATH, INTEGRIN-α and INTEGRIN-β EXPRESSIONS IN DU145 PROSTATE CANCER CELL LINE”. Kocatepe Tıp Dergisi, vol. 25, no. 4, 2024, pp. 420-8, doi:10.18229/kocatepetip.1402118.
Vancouver Karaca Ç, Arıkan Söylemez ES, Aslan E, Fırat F, Söylemez Z. COMPARISON OF THE EFFECTS OF DOCETAXEL and AMYGDALIN TREATMENT ON CELL DEATH, INTEGRIN-α and INTEGRIN-β EXPRESSIONS IN DU145 PROSTATE CANCER CELL LINE. KTD. 2024;25(4):420-8.

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