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Opioid Receptor Expression in Colorectal Cancer: A Nested Matched Case-Control Study.
Amparo Belltall1,2, Guido Mazzinari1,2,3, Iris Garrido-Cano3,4,5
1Research Group in Perioperative Medicine, Hospital Universitario y Politécnico la Fe, Valencia, Spain.
Perioperative opioid receptor expression in colorectal cancer tissues was significantly increased but did not differ by recurrence. This suggests opioid receptors may not influence cancer recurrence in stage II/III colorectal cancer patients.
Area of Science:
- Oncology
- Anesthesiology
- Molecular Biology
Background:
- Perioperative anesthetic management's impact on cancer progression is under investigation.
- The role of perioperative opioids in cancer recurrence remains controversial.
- This study investigates opioid receptor expression in colorectal cancer tissues.
Purpose of the Study:
- To assess differential expression of µ-opioid receptor (MOR) and Opioid Growth Factor Receptor (OGFR) between healthy and tumor tissues in stage II/III colorectal cancer patients.
- To explore the relationship between opioid receptor expression and cancer recurrence.
- To analyze the cAMP-PKA pathway and validate findings using TCGA-GTEx databases.
Main Methods:
- Retrospective cohort study with propensity-score matched case-control analysis.
- Immunohistochemistry (IHC) to measure MOR and OGFR expression in tumor and healthy tissues.
- Analysis of cAMP, PKA, and in silico data from TCGA-GTEx.
Main Results:
- Significantly higher MOR and OGFR expression in tumor tissues compared to healthy tissues (P<0.001).
- No significant differences in MOR, OGFR, cAMP, or PKA expression based on recurrence status.
- TCGA-GTEx data confirmed increased MOR and OGFR expression in tumor samples, with a skewed MOR distribution.
Conclusions:
- MOR and OGFR expression are significantly increased in stage II/III colorectal cancer tissues.
- Increased MOR and OGFR expression in tumor tissues do not correlate with cancer recurrence.
- The cAMP-PKA pathway is not differentially expressed between tumor and healthy tissues or by recurrence status.
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