Morphine Analgesia, Cannabinoid Receptor 2, and Opioid Growth Factor Receptor Cancer Tissue Expression Improve Survival after Pancreatic Cancer Surgery
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
NV18-03-00470
Ministry of Health
BBMRI - LM2018125, NCMG - LM2023067, EATRIS-CZ - LM2018133
Ministry of Youth and Sports
Programme EXCELES, ID Project No. LX22NPO5102
European Union - Next Generation EU
LF 2023_006
Palacky University Olomouc
PubMed
37627066
PubMed Central
PMC10452720
DOI
10.3390/cancers15164038
PII: cancers15164038
Knihovny.cz E-zdroje
- Klíčová slova
- cancer recurrence, cannabinoid receptors, morphine, opioid receptors, pancreatic cancer, pancreatic surgery, patient survival, piritramide, postoperative analgesia,
- Publikační typ
- časopisecké články MeSH
Pancreatic cancer (PDAC) has a poor prognosis despite surgical removal and adjuvant therapy. Additionally, the effects of postoperative analgesia with morphine and piritramide on survival among PDAC patients are unknown, as are their interactions with opioid/cannabinoid receptor gene expressions in PDAC tissue. Cancer-specific survival data for 71 PDAC patients who underwent radical surgery followed by postoperative analgesia with morphine (n = 48) or piritramide (n = 23) were therefore analyzed in conjunction with opioid/cannabinoid receptor gene expressions in the patients' tumors. Receptor gene expressions were determined using the quantitative real-time polymerase chain reaction. Patients receiving morphine had significantly longer cancer-specific survival (CSS) than those receiving piritramide postoperative analgesia (median 22.4 vs. 15 months; p = 0.038). This finding was supported by multivariate modelling (p < 0.001). The morphine and piritramide groups had similar morphine equipotent doses, receptor expression, and baseline characteristics. The opioid/cannabinoid receptor gene expression was analyzed in a group of 130 pancreatic cancer patients. Of the studied receptors, high cannabinoid receptor 2 (CB2) and opioid growth factor receptor (OGFR) gene expressions have a positive influence on the length of overall survival (OS; p = 0.029, resp. p = 0.01). Conversely, high delta opioid receptor gene expression shortened OS (p = 0.043). Multivariate modelling indicated that high CB2 and OGFR expression improved OS (HR = 0.538, p = 0.011, resp. HR = 0.435, p = 0.001), while high OPRD receptor expression shortened OS (HR = 2.264, p = 0.002). Morphine analgesia, CB2, and OGFR cancer tissue gene expression thus improved CSS resp. OS after radical PDAC surgery, whereas delta opioid receptor expression shortened OS.
Cancer Research Czech Republic Foundation 779 00 Olomouc Czech Republic
Department of Anaesthesia and Intensive Care Ringerike Hospital 3511 Hønefoss Norway
Department of Anesthesiology and Intensive Medicine Landesklinikum Amstetten 3300 Amstetten Austria
Department of Emergency Medicine The Tomas Bata Regional Hospital in Zlin 762 75 Zlin Czech Republic
Laboratory of Experimental Medicine Olomouc University Hospital 779 00 Olomouc Czech Republic
Zobrazit více v PubMed
Rawla P., Sunkara T., Gaduputi V. Epidemiology of Pancreatic Cancer: Global Trends, Etiology and Risk Factors. World J. Oncol. 2019;10:10–27. doi: 10.14740/wjon1166. PubMed DOI PMC
Latenstein A.E.J., van Roessel S., van der Geest L.G.M., Bonsing B.A., Dejong C.H.C., Groot Koerkamp B., de Hingh I.H.J.T., Homs M.Y.V., Klaase J.M., Lemmens V., et al. Conditional Survival After Resection for Pancreatic Cancer: A Population-Based Study and Prediction Model. Ann. Surg. Oncol. 2020;27:2516–2524. doi: 10.1245/s10434-020-08235-w. PubMed DOI PMC
Call T.R., Pace N.L., Thorup D.B., Maxfield D., Chortkoff B., Christensen J., Mulvihill S.J. Factors Associated with Improved Survival after Resection of Pancreatic Adenocarcinoma: A Multivariable Model. Anesthesiology. 2015;122:317–324. doi: 10.1097/ALN.0000000000000489. PubMed DOI
Kobi M., Veillette G., Narurkar R., Sadowsky D., Paroder V., Shilagani C., Gilet A., Flusberg M. Imaging and Management of Pancreatic Cancer. Semin. Ultrasound CT MR. 2020;41:139–151. doi: 10.1053/j.sult.2019.12.003. PubMed DOI
Loveday B.P., Lipton L., Thomson B.N. Pancreatic Cancer: An Update on Diagnosis and Management. Aust. J. Gen. Gen. Pract. 2019;48:826–831. doi: 10.31128/AJGP-06-19-4957. PubMed DOI
McGuigan A., Kelly P., Turkington R.C., Jones C., Coleman H.G., McCain R.S. Pancreatic Cancer: A Review of Clinical Diagnosis, Epidemiology, Treatment and Outcomes. World J. Gastroenterol. 2018;24:4846–4861. doi: 10.3748/wjg.v24.i43.4846. PubMed DOI PMC
Cummings K.C., Xu F., Cummings L.C., Cooper G.S. A Comparison of Epidural Analgesia and Traditional Pain Management Effects on Survival and Cancer Recurrence after Colectomy: A Population-Based Study. Anesthesiology. 2012;116:797–806. doi: 10.1097/ALN.0b013e31824674f6. PubMed DOI
Xu Z.-Z., Li H.-J., Li M.-H., Huang S.-M., Li X., Liu Q.-H., Li J., Li X.-Y., Wang D.-X., Sessler D.I. Epidural Anesthesia-Analgesia and Recurrence-Free Survival after Lung Cancer Surgery: A Randomized Trial. Anesthesiology. 2021;135:419–432. doi: 10.1097/ALN.0000000000003873. PubMed DOI
Sessler D.I. Does Regional Analgesia Reduce the Risk of Cancer Recurrence? A Hypothesis. Eur. J. Cancer Prev. 2008;17:269–272. doi: 10.1097/CEJ.0b013e3282f0c005. PubMed DOI
Havlik R., Srovnal J., Klos D., Benedikova A., Lovecek M., Ghothim M., Cahova D., Neoral C., Hajduch M. Occult Tumour Cells in Peritoneal Lavage Are a Negative Prognostic Factor in Pancreatic Cancer. Biomed. Pap. Med. Fac. Palacky Univ. Olomouc Czech Repub. 2013;157:233–238. doi: 10.5507/bp.2012.061. PubMed DOI
Park Y., Jun H.R., Choi H.W., Hwang D.W., Lee J.H., Song K.B., Lee W., Kwon J., Ha S.H., Jun E., et al. Circulating Tumour Cells as an Indicator of Early and Systemic Recurrence after Surgical Resection in Pancreatic Ductal Adenocarcinoma. Sci. Rep. 2021;11:1644. doi: 10.1038/s41598-020-80383-1. PubMed DOI PMC
Lu Y., Wang P., Peng J., Wang X., Zhu Y., Shen N. Meta-Analysis Reveals the Prognostic Value of Circulating Tumour Cells Detected in the Peripheral Blood in Patients with Non-Metastatic Colorectal Cancer. Sci. Rep. 2017;7:905. doi: 10.1038/s41598-017-01066-y. PubMed DOI PMC
Stejskal P., Srovnal J., Berta E., Rehulkova A., Vecera L., Haiduk F., Michalek P., Hajduch M. Abstract 1956: Perioperative Opioid Analgesia Affects the Circulating Tumor Cells Levels in Colorectal Cancer Patients. Cancer Res. 2022;82:1956. doi: 10.1158/1538-7445.AM2022-1956. DOI
Srovnal J., Berta E., Rehulkova A., Vidlarova M., Prasil P., Vecera L., Stourac P., Kourilova P., Hajduch M. Abstract B41: Piritramide Analgesia Reduces CEA MRNA-Positive Circulating Tumor Cells’ Presence Compared to Morphine and Epidural Analgesia Following Radical Colon Cancer Surgery. Clin. Cancer Res. 2020;26:B41. doi: 10.1158/1557-3265.LiqBiop20-B41. DOI
Vidlarova M., Berta E., Prasil P., Prokopova A., Gurska S., Khoylou M., Rehulkova A., Kourilova P., Chudacek J., Szkorupa M., et al. Cannabinoid Receptor 2 Expression in Early-Stage Non-Small Cell Lung Cancers Identifies Patients with Good Prognosis and Longer Survival. Transl. Lung Cancer Res. 2022;11:2040–2050. doi: 10.21037/tlcr-22-247. PubMed DOI PMC
Xu X., Liu Y., Huang S., Liu G., Xie C., Zhou J., Fan W., Li Q., Wang Q., Zhong D., et al. Overexpression of Cannabinoid Receptors CB1 and CB2 Correlates with Improved Prognosis of Patients with Hepatocellular Carcinoma. Cancer Genet. Cytogenet. 2006;171:31–38. doi: 10.1016/j.cancergencyto.2006.06.014. PubMed DOI
Carracedo A., Lorente M., Egia A., Blázquez C., García S., Giroux V., Malicet C., Villuendas R., Gironella M., González-Feria L., et al. The Stress-Regulated Protein P8 Mediates Cannabinoid-Induced Apoptosis of Tumor Cells. Cancer Cell. 2006;9:301–312. doi: 10.1016/j.ccr.2006.03.005. PubMed DOI
Vecera L., Gabrhelik T., Prasil P., Stourac P. The Role of Cannabinoids in the Treatment of Cancer. Bratisl. Lek. Listy. 2020;121:79–95. doi: 10.4149/BLL_2020_012. PubMed DOI
Solinas M., Massi P., Cantelmo A.R., Cattaneo M.G., Cammarota R., Bartolini D., Cinquina V., Valenti M., Vicentini L.M., Noonan D.M., et al. Cannabidiol Inhibits Angiogenesis by Multiple Mechanisms. Br. J. Pharmacol. 2012;167:1218–1231. doi: 10.1111/j.1476-5381.2012.02050.x. PubMed DOI PMC
Pisanti S., Picardi P., D’Alessandro A., Laezza C., Bifulco M. The Endocannabinoid Signaling System in Cancer. Trends Pharmacol. Sci. 2013;34:273–282. doi: 10.1016/j.tips.2013.03.003. PubMed DOI
Zhu L.X., Sharma S., Stolina M., Gardner B., Roth M.D., Tashkin D.P., Dubinett S.M. Delta-9-Tetrahydrocannabinol Inhibits Antitumor Immunity by a CB2 Receptor-Mediated, Cytokine-Dependent Pathway. J. Immunol. 2000;165:373–380. doi: 10.4049/jimmunol.165.1.373. PubMed DOI
Michalski C.W., Oti F.E., Erkan M., Sauliunaite D., Bergmann F., Pacher P., Batkai S., Müller M.W., Giese N.A., Friess H., et al. Cannabinoids in Pancreatic Cancer: Correlation with Survival and Pain. Int. J. Cancer. 2008;122:742–750. doi: 10.1002/ijc.23114. PubMed DOI PMC
Zhang H., Qu M., Gorur A., Sun Z., Cata J.P., Chen W., Miao C. Association of Mu-Opioid Receptor (MOR) Expression and Opioids Requirement with Survival in Patients with Stage I-III Pancreatic Ductal Adenocarcinoma. Front. Oncol. 2021;11:686877. doi: 10.3389/fonc.2021.686877. PubMed DOI PMC
Zagon I.S., Smith J.P., McLaughlin P.J. Human Pancreatic Cancer Cell Proliferation in Tissue Culture Is Tonically Inhibited by Opioid Growth Factor. Int. J. Oncol. 1999;14:577–584. doi: 10.3892/ijo.14.3.577. PubMed DOI
Haque M.R., Barlass U., Armstrong A., Shaikh M., Bishehsari F. Novel Role of the Mu-Opioid Receptor in Pancreatic Cancer: Potential Link between Opioid Use and Cancer Progression. Mol. Cell. Biochem. 2022;477:1339–1345. doi: 10.1007/s11010-022-04377-5. PubMed DOI
Shakhar G., Ben-Eliyahu S. Potential Prophylactic Measures against Postoperative Immunosuppression: Could They Reduce Recurrence Rates in Oncological Patients? Ann. Surg. Oncol. 2003;10:972–992. doi: 10.1245/aso.2003.02.007. PubMed DOI
Stamer U., Mpasios N., Stüber F., Laubenthal H., Maier C. Postoperative Schmerztherapie in Deutschland Ergebnisse einer Umfrage. Anaesthesist. 2002;51:248–257. doi: 10.1007/s00101-002-0288-7. PubMed DOI
Kinstner C., Likar R., Sandner-Kiesling A., Hutschala D., Pipam W., Gustorff B. Qualität der postoperativen Schmerztherapie in Österreich. Anaesthesist. 2011;60:827. doi: 10.1007/s00101-011-1911-2. PubMed DOI
Gabrhelík T., Pieran M. Léčba Pooperační Bolesti. Interní Medicína Pro Praxi. 2012;14:23–25.
Gramke H.-F., de Rijke J.M., van Kleef M., Raps F., Kessels A.G.H., Peters M.L., Sommer M., Marcus M.A.E. The Prevalence of Postoperative Pain in a Cross-Sectional Group of Patients after Day-Case Surgery in a University Hospital. Clin. J. Pain. 2007;23:543–548. doi: 10.1097/AJP.0b013e318074c970. PubMed DOI
Janssen P.A. Pirinitramide (R 3365), a Potent Analgesic with Unusual Chemical Structure. J. Pharm. Pharmacol. 1961;13:513–530. doi: 10.1111/j.2042-7158.1961.tb11864.x. PubMed DOI
Kumar N., Rowbotham D.J. Piritramide. Br. J. Anaesth. 1999;82:3–5. doi: 10.1093/bja/82.1.3. PubMed DOI
Hinrichs M., Weyland A., Bantel C. Piritramid. Schmerz. 2017;31:345–352. doi: 10.1007/s00482-017-0197-y. PubMed DOI
Kay B. A Clinical Investigation of Piritramide in the Treatment of Postoperative Pain. Br. J. Anaesth. 1971;43:1167–1171. doi: 10.1093/bja/43.12.1167. PubMed DOI
Gottschalk A., Sharma S., Ford J., Durieux M.E., Tiouririne M. Review Article: The Role of the Perioperative Period in Recurrence after Cancer Surgery. Anesth. Analg. 2010;110:1636–1643. doi: 10.1213/ANE.0b013e3181de0ab6. PubMed DOI
Harimaya Y., Koizumi K., Andoh T., Nojima H., Kuraishi Y., Saiki I. Potential Ability of Morphine to Inhibit the Adhesion, Invasion and Metastasis of Metastatic Colon 26-L5 Carcinoma Cells. Cancer Lett. 2002;187:121–127. doi: 10.1016/S0304-3835(02)00360-9. PubMed DOI
Zagon I.S., Rahn K.A., McLaughlin P.J. Opioids and Migration, Chemotaxis, Invasion, and Adhesion of Human Cancer Cells. Neuropeptides. 2007;41:441–452. doi: 10.1016/j.npep.2007.08.002. PubMed DOI
Gupta K., Kshirsagar S., Chang L., Schwartz R., Law P.-Y., Yee D., Hebbel R.P. Morphine Stimulates Angiogenesis by Activating Proangiogenic and Survival-Promoting Signaling and Promotes Breast Tumor Growth. Cancer Res. 2002;62:4491–4498. PubMed
Ustun F., Durmus-Altun G., Altaner S., Tuncbilek N., Uzal C., Berkarda S. Evaluation of Morphine Effect on Tumour Angiogenesis in Mouse Breast Tumour Model, EATC. Med. Oncol. 2011;28:1264–1272. doi: 10.1007/s12032-010-9573-5. PubMed DOI
Koodie L., Ramakrishnan S., Roy S. Morphine Suppresses Tumor Angiogenesis through a HIF-1alpha/P38MAPK Pathway. Am. J. Pathol. 2010;177:984–997. doi: 10.2353/ajpath.2010.090621. PubMed DOI PMC
Zagon I.S., McLaughlin P.J. Opioid Growth Factor and the Treatment of Human Pancreatic Cancer: A Review. World J. Gastroenterol. 2014;20:2218–2223. doi: 10.3748/wjg.v20.i9.2218. PubMed DOI PMC
Zagon I.S., Verderame M.F., Hankins J., McLaughlin P.J. Overexpression of the Opioid Growth Factor Receptor Potentiates Growth Inhibition in Human Pancreatic Cancer Cells. Int. J. Oncol. 2007;30:775–783. doi: 10.3892/ijo.30.4.775. PubMed DOI
Zagon I.S., Smith J.P., Conter R., McLaughlin P.J. Identification and Characterization of Opioid Growth Factor Receptor in Human Pancreatic Adenocarcinoma. Int. J. Mol. Med. 2000;5:77–84. PubMed
Falk W., Magnuson A., Eintrei C., Henningsson R., Myrelid P., Matthiessen P., Gupta A. Comparison between Epidural and Intravenous Analgesia Effects on Disease-Free Survival after Colorectal Cancer Surgery: A Randomised Multicentre Controlled Trial. Br. J. Anaesth. 2021;127:65–74. doi: 10.1016/j.bja.2021.04.002. PubMed DOI PMC
Prasil P., Berta E., Srovnal J., Gabrhelik T., Adamus M., Hajduch M. Morphinebut Not Piritramide-Based Postoperative Analgesia Negatively Influences Levels of Circulating Tumor Cells and Patients’ Survival Following Colorectal Cancer Surgery: 14AP6-1. Eur. J. Anaesthesiol. EJA. 2014;31:229. doi: 10.1097/00003643-201406001-00661. DOI
Ravi J., Sneh A., Shilo K., Nasser M.W., Ganju R.K. FAAH Inhibition Enhances Anandamide Mediated Anti-Tumorigenic Effects in Non-Small Cell Lung Cancer by Downregulating the EGF/EGFR Pathway. Oncotarget. 2014;5:2475–2486. doi: 10.18632/oncotarget.1723. PubMed DOI PMC
Sierra S., Gupta A., Gomes I., Fowkes M., Ram A., Bobeck E.N., Devi L.A. Targeting Cannabinoid 1 and Delta Opioid Receptor Heteromers Alleviates Chemotherapy-Induced Neuropathic Pain. ACS Pharmacol. Transl. Sci. 2019;2:219–229. doi: 10.1021/acsptsci.9b00008. PubMed DOI PMC
Page G.G. Immunologic Effects of Opioids in the Presence or Absence of Pain. J. Pain Symptom Manag. 2005;29:S25–S31. doi: 10.1016/j.jpainsymman.2005.01.006. PubMed DOI
Martinez L., Ekman E., Nakhla N. Perioperative Opioid-Sparing Strategies: Utility of Conventional NSAIDs in Adults. Clin. Ther. 2019;41:2612–2628. doi: 10.1016/j.clinthera.2019.10.002. PubMed DOI
Mulita F., Karpetas G., Liolis E., Vailas M., Tchabashvili L., Maroulis I. Comparison of Analgesic Efficacy of Acetaminophen Monotherapy versus Acetaminophen Combinations with Either Pethidine or Parecoxib in Patients Undergoing Laparoscopic Cholecystectomy: A Randomized Prospective Study. Med. Glas. 2021;18:27–32. doi: 10.17392/1245-21. PubMed DOI
Petrelli F., Tomasello G., Ghidini M., Lonati V., Passalacqua R., Barni S. Disease-Free Survival Is Not a Surrogate Endpoint for Overall Survival in Adjuvant Trials of Pancreatic Cancer: A Systematic Review of Randomized Trials. HPB. 2017;19:944–950. doi: 10.1016/j.hpb.2017.07.005. PubMed DOI