Melatonin, p21, p27, p53, p57, MDM2 ve KRAS Genlerinin modülasyonu yoluyla Pankreas Karsinomu Hücrelerinin (PANC-1) Cisplatin ve Cetuximab'a Kemosensitivitesini Artırır

Yıl 2021, Cilt: 10 Sayı: 2, 275 - 282, 31.12.2021

Cihan Gür , Seçkin Özkanlar

https://doi.org/10.46810/tdfd.998059

Öz

Tek başına veya kombinasyon halinde melatonin, setuksimab ve sisplatin tedavilerinin, hücre canlılığı ve gen ekspresyonları yoluyla duktal hücre kaynaklı bir insan pankreas karsinomunun PANC-1 hücreleri üzerindeki etkilerini araştırdık. PANC-1 hücrelerine kimyasallar uygulandıktan sonra hücreler 48 saat inkübasyona bırakıldı. İnkübasyon sonunda maddelerin hücre canlılığı üzerindeki metabolik etkileri MTT tahlili ile ölçüldü. p21, p27, p53, p57, MDM2 ve KRAS'ın gen ifadeleri RT-PCR ile belirlendi. Sisplatin veya setuksimab ile kombine melatonin kullanımı, p21 ve p57 genlerini arttırdı ve KRAS genini azalttı. Ayrıca, setuksimab ile kombine edilen melatonin, tek başına setuksimab ile karşılaştırıldığında p27 gen ekspresyonunu arttırdı ve hücre canlılığını azalttı. Hücre canlılığı, sisplatin ve sisplatin artı melatonin ve/veya setuksimab gruplarında en düşüktü. p53, sisplatin gruplarında en yüksek iken, sisplatin artı melatonin, tek başına sisplatine kıyasla p53 genini ve onun otoregülatör MDM2 genini azalttı. Sonuç olarak, sisplatin ve setuksimab ile kombinasyon halinde melatonin, tümör baskılayıcı genler p21, p27 ve p57 ile birlikte onkojenik gen KRAS'ın bir modülasyonunu arttırır, bu da melatoninin pankreas duktal adenokarsinomunun kombinasyon tedavisinde terapötik bir yaklaşım olarak potansiyelini ortaya koyar.

Anahtar Kelimeler

Cetuximab, sisplatin, melatonin, onkogenler, pankreas kanseri, tümör baskılayıcı genler.

Destekleyen Kurum

Atatürk Üniversitesi Bilimsel Araştırmalar Projeleri

Proje Numarası

PRJ2014/154

Melatonin Enhances the Chemosensitivity of Pancreatic Carcinoma Cells (PANC-1) to Cisplatin and Cetuximab through modulation of p21, p27, p53, p57, MDM2 and KRAS Genes

Öz

We investigated the effects of melatonin, cetuximab and cisplatin treatments alone or in combination on PANC-1 cells from a human pancreatic carcinoma of ductal cell origin through cell viability and gene expressions. The cells were left for 48 h incubation after applying chemicals on the PANC-1 cells. The metabolic effects of the substances on cell viability at the end of incubation were measured by MTT assay. The gene expressions of p21, p27, p53, p57, MDM2 and KRAS were determined by RT-PCR. The use of melatonin combined with cisplatin or cetuximab increased p21 and p57 genes and decreased KRAS gene. Furthermore, melatonin combined with cetuximab increased p27 gene expression and decreased the cell viability compared to cetuximab alone. The cell viability was the lowest in cisplatin and cisplatin plus melatonin and/or cetuximab groups. The p53 were highest in the cisplatin groups while cisplatin plus melatonin decreased the p53 gene and its autoregulator MDM2 gene compared to cisplatin alone. In conclusion, melatonin in combinations with cisplatin and cetuximab enhances the tumor suppressor genes p21, p27 and p57 along with a modulation of the oncogenic gene KRAS suggesting the potential of melatonin as a therapeutic approach in combination therapy of pancreatic ductal adenocarcinoma.

Anahtar Kelimeler

Cetuximab, cisplatin, melatonin, oncogenes, pancreatic cancer, tumor suppressor genes.

Proje Numarası

PRJ2014/154

Kaynakça

• Referans1 Lippi G, Mattiuzzi C. The global burden of pancreatic cancer. Arch Med Sci. 2020;16(4):820-4.
• Referans2 Kong F, Liu X, Zhou Y, Hou X, He J, Li Q, et al. Downregulation of METTL14 increases apoptosis and autophagy induced by cisplatin in pancreatic cancer cells. The International Journal of Biochemistry & Cell Biology. 2020;122:105731.
• Referans3 Han H, Hou Y, Chen X, Zhang P, Kang M, Jin Q, et al. Metformin-Induced Stromal Depletion to Enhance the Penetration of Gemcitabine-Loaded Magnetic Nanoparticles for Pancreatic Cancer Targeted Therapy. Journal of the American Chemical Society. 2020;142(10):4944-54.
• Referans4 Chandana S, Babiker HM, Mahadevan D. Therapeutic trends in pancreatic ductal adenocarcinoma (PDAC). Expert Opin Investig Drugs. 2019;28(2):161-77.
• Referans5 Miller AL, Garcia PL, Yoon KJ. Developing effective combination therapy for pancreatic cancer: An overview. Pharmacol Res. 2020;155:104740.
• Referans6 Kaneko T, Sugimori K, Tozuka Y, Fukushima T, Okada K, Oka H, et al. Combination chemotherapy with gemcitabine and nab-paclitaxel for a metastatic pancreatic ductal adenocarcinoma patient undergoing hemodialysis. Clin J Gastroenterol. 2019;12(5):484-9.
• Referans7 Xie H, Liu J, Ogden JR, Yin J, Jatoi A, Hubbard JM, et al. Survival Benefit of Combination Chemotherapy in Elderly Patients With Metastatic Pancreatic Ductal Adenocarcinoma. Am J Clin Oncol. 2020;43(8):586-90.
• Referans8 Chen B, Xu M, Zhang H, Wang J-x, Zheng P, Gong L, et al. Cisplatin-induced non-apoptotic death of pancreatic cancer cells requires mitochondrial cyclophilin-D-p53 signaling. Biochemical and biophysical research communications. 2013;437(4):526-31.
• Referans9 Ergun Y, Ozdemir NY, Guner EK, Esin E, Sendur MA, Koksoy EB, et al. Comparison of gemcitabine monotherapy with gemcitabine and cisplatin combination in metastatic pancreatic cancer: a retrospective analysis. J BUON. 2018;23:116-21.
• Referans10 Bragado P, Armesilla A, Silva A, Porras A. Apoptosis by cisplatin requires p53 mediated p38α MAPK activation through ROS generation. Apoptosis. 2007;12(9):1733-42.
• Referans11 Yin F, Zhang Q, Dong Z, Hu J, Ma Z. LncRNA HOTTIP Participates in Cisplatin Resistance of Tumor Cells by Regulating miR-137 Expression in Pancreatic Cancer. OncoTargets and therapy. 2020;13:2689.
• Referans12 Jimeno A, Rubio-Viqueira B, Amador ML, Oppenheimer D, Bouraoud N, Kulesza P, et al. Epidermal growth factor receptor dynamics influences response to epidermal growth factor receptor targeted agents. Cancer research. 2005;65(8):3003-10.
• Referans13 Cheng Y-d, Yang H, Chen G-q, Zhang Z-c. Molecularly targeted drugs for metastatic colorectal cancer. Drug design, development and therapy. 2013;7:1315.
• Referans14 Ruiz-Rabelo J, Vázquez R, Arjona Á, Perea D, Montilla P, Túnez I, et al. Improvement of capecitabine antitumoral activity by melatonin in pancreatic cancer. Pancreas. 2011;40(3):410-4.
• Referans15 Li W, Wu J, Li Z, Zhou Z, Zheng C, Lin L, et al. Melatonin induces cell apoptosis in Mia PaCa-2 cells via the suppression of nuclear factor-κB and activation of ERK and JNK: A novel therapeutic implication for pancreatic cancer. Oncology reports. 2016;36(5):2861-7.
• Referans16 Martín‐Renedo J, Mauriz JL, Jorquera F, Ruiz‐Andrés O, González P, González‐Gallego J. Melatonin induces cell cycle arrest and apoptosis in hepatocarcinoma HepG2 cell line. Journal of pineal research. 2008;45(4):532-40.
• Referans17 Leja-Szpak A, Nawrot-Porabka K, Goralska M, Jastrzebska M, Link-Lenczowski P, Bonior J, et al. Melatonin and its metabolite N1-acetyl-N2-formyl-5-methoxykynuramine (afmk) enhance chemosensitivity to gemcitabine in pancreatic carcinoma cells (PANC-1). Pharmacol Rep. 2018;70(6):1079-88.
• Referans18 Kamisawa T, Wood LD, Itoi T, Takaori K. Pancreatic cancer. The Lancet. 2016;388(10039):73-85.
• Referans19 Neoptolemos J, Dunn J, Stocken D, Almond J, Link K, Beger H, et al. Adjuvant chemoradiotherapy and chemotherapy in resectable pancreatic cancer: a randomised controlled trial. The Lancet. 2001;358(9293):1576-85.
• Referans20 Mezencev R, Matyunina LV, Wagner GT, McDonald JF. Acquired resistance of pancreatic cancer cells to cisplatin is multifactorial with cell context-dependent involvement of resistance genes. Cancer Gene Ther. 2016;23(12):446-53.
• Referans21 Chen W, Shen X, Xia X, Xu G, Ma T, Bai X, et al. NSC 74859‐mediated inhibition of STAT 3 enhances the anti‐proliferative activity of cetuximab in hepatocellular carcinoma. Liver International. 2012;32(1):70-7.
• Referans22 Uguz AC, Cig B, Espino J, Bejarano I, Naziroglu M, Rodríguez AB, et al. Melatonin potentiates chemotherapy‐induced cytotoxicity and apoptosis in rat pancreatic tumor cells. Journal of pineal research. 2012;53(1):91-8.
• Referans23 Fang Z, Jung KH, Yan HH, Kim SJ, Rumman M, Park JH, et al. Melatonin Synergizes with Sorafenib to Suppress Pancreatic Cancer via Melatonin Receptor and PDGFR-beta/STAT3 Pathway. Cell Physiol Biochem. 2018;47(5):1751-68.
• Referans24 Geske F, Nelson AC, Lieberman R, Strange R, Sun T, Gerschenson L. DNA repair is activated in early stages of p53-induced apoptosis. Cell Death & Differentiation. 2000;7(4):393-401.
• Referans25 Slebos RJ, Hoppin JA, Tolbert PE, Holly EA, Brock JW, Zhang RH, et al. K-ras and p53 in pancreatic cancer: association with medical history, histopathology, and environmental exposures in a population-based study. Cancer Epidemiology and Prevention Biomarkers. 2000;9(11):1223-32.
• Referans26 Lee Y-S, Chin Y-T, Yang Y-CS, Wei P-L, Wu H-C, Shih A, et al. The combination of tetraiodothyroacetic acid and cetuximab inhibits cell proliferation in colorectal cancers with different K-ras status. Steroids. 2016;111:63-70.
• Referans27 Song J, Ma S-J, Luo J-H, Zhang H, Wang R-X, Liu H, et al. Melatonin induces the apoptosis and inhibits the proliferation of human gastric cancer cells via blockade of the AKT/MDM2 pathway. Oncology reports. 2018;39(4):1975-83.
• Referans28 Gelaleti GB, Borin TF, Maschio-Signorini LB, Moschetta MG, Jardim-Perassi BV, Calvinho GB, et al. Efficacy of melatonin, IL-25 and siIL-17B in tumorigenesis-associated properties of breast cancer cell lines. Life sciences. 2017;183:98-109.
• Referans29 Chi S-W, Lee S-H, Kim D-H, Ahn M-J, Kim J-S, Woo J-Y, et al. Structural details on mdm2-p53 interaction. Journal of Biological Chemistry. 2005;280(46):38795-802.
• Referans30 Azmi AS, Aboukameel A, Banerjee S, Wang Z, Mohammad M, Wu J, et al. MDM2 inhibitor MI-319 in combination with cisplatin is an effective treatment for pancreatic cancer independent of p53 function. European Journal of Cancer. 2010;46(6):1122-31.
• Referans31 Proietti S, Cucina A, Dobrowolny G, D'Anselmi F, Dinicola S, Masiello MG, et al. Melatonin down‐regulates MDM 2 gene expression and enhances p53 acetylation in MCF‐7 cells. Journal of pineal research. 2014;57(1):120-9.
• Referans32 Proietti S, Cucina A, D’Anselmi F, Dinicola S, Pasqualato A, Lisi E, et al. Melatonin and vitamin D3 synergistically down‐regulate Akt and MDM2 leading to TGFβ‐1‐dependent growth inhibition of breast cancer cells. Journal of pineal research. 2011;50(2):150-8.
• Referans33 El-Deiry WS. p21 [WAF1] mediates cell-cycle inhibition, relevant to cancer suppression and therapy. Cancer research. 2016;76(18):5189-91.
• Referans34 Thapa RK, Choi JY, Gupta B, Ramasamy T, Poudel BK, Ku SK, et al. Liquid crystalline nanoparticles encapsulating cisplatin and docetaxel combination for targeted therapy of breast cancer. Biomaterials science. 2016;4(9):1340-50.
• Referans35 Terzuoli E, Nannelli G, Frosini M, Giachetti A, Ziche M, Donnini S. Inhibition of cell cycle progression by the hydroxytyrosol–cetuximab combination yields enhanced chemotherapeutic efficacy in colon cancer cells. Oncotarget. 2017;8(47):83207.
• Referans36 Nooshinfar E, Bashash D, Safaroghli-Azar A, Bayati S, Rezaei-Tavirani M, Ghaffari SH, et al. Melatonin promotes ATO-induced apoptosis in MCF-7 cells: Proposing novel therapeutic potential for breast cancer. Biomedicine & Pharmacotherapy. 2016;83:456-65.
• Referans37 Juuti A, Nordling S, Louhimo J, Lundin J, Von Boguslawski K, Haglund C. Loss of p27 expression is associated with poor prognosis in stage I–II pancreatic cancer. Oncology. 2003;65(4):371-7.
• Referans38 Zhu F, Dai SN, Xu DL, Hou CQ, Liu TT, Chen QY, et al. EFNB2 facilitates cell proliferation, migration, and invasion in pancreatic ductal adenocarcinoma via the p53/p21 pathway and EMT. Biomed Pharmacother. 2020;125:109972.
• Referans39 Ayyagari VN, Hsieh T-hJ, Diaz-Sylvester PL, Brard L. Evaluation of the cytotoxicity of the Bithionol-cisplatin combination in a panel of human ovarian cancer cell lines. BMC cancer. 2017;17(1):49.
• Referans40 Li WY, Li Q, Jing L, Wu T, Han LL, Wang Y, et al. P57‐mediated autophagy promotes the efficacy of EGFR inhibitors in hepatocellular carcinoma. Liver International. 2019;39(1):147-57.
• Referans41 Guo H, Tian T, Nan K, Wang W. p57: A multifunctional protein in cancer. International journal of oncology. 2010;36(6):1321-9.
• Referans42 Lanfredini S, Thapa A, O'Neill E. RAS in pancreatic cancer. Biochem Soc Trans. 2019;47(4):961-72.
• Referans43 Oliverius M, Flasarova D, Mohelnikova-Duchonova B, Ehrlichova M, Hlavac V, Kocik M, et al. KRAS pathway expression changes in pancreatic cancer models by conventional and experimental taxanes. Mutagenesis. 2019;34(5-6):403-11.