Evaluation of Mu Opioid Receptor Expression via Immunohistochemistry in Various Tumor Types

Main Article Content

Jolanta Jedrzkiewicz Tyler R. Call Sheryl R. Tripp Benjamin L. Witt

Abstract

Up-regulation of mu-opioid receptors (MOR) in certain tumors has been reported. Understanding which tumors have up-regulation of MOR could prove helpful in this field of research if indeed opioids have growth effects on certain tumor cells. We attempt to create a Mu-score system that would quantify the mu receptor density of various tumors. Our study investigates immunohistochemical analysis of various tumor tissues with two commercially available opioid antibodies, both of which showed patchy reactivity within tumor tissue and nonspecific background staining. These findings suggest that currently available immunohistochemical stains are of limited utility both in assessing tumor tissue MOR density and in creating the proposed Mu-score system.

Article Details

How to Cite
JEDRZKIEWICZ, Jolanta et al. Evaluation of Mu Opioid Receptor Expression via Immunohistochemistry in Various Tumor Types. Medical Research Archives, [S.l.], v. 2, n. 2, sep. 2015. ISSN 2375-1924. Available at: <https://esmed.org/MRA/mra/article/view/195>. Date accessed: 22 dec. 2024.
Keywords
opioid receptor; immunohistochemistry; opioid receptor in tumors
Section
Research Articles

References

1. Sessler DI, Ben-Eliyahu S, Mascha EJ, Parat MO, Buggy DJ. Can regional analgesia reduce the risk of recurrence after breast cancer?: Methodology of a multicenter randomized trial. Contemporary Clinical Trials. 2008;29( 4):517-526.

2. Welden B, Gates G, Mallari R, Garrett N. Effects of anesthetics and analgesics on natural killer cell activity. AANA Journal 2009;77(4):287-292.

3. Gupta K, Kshirsagar S, Chang L, Schwartz R, Law PY, Hebbel RP. Morphine stimulates angiogenesis by activating proangiogenic and survival-promoting signaling and promotes breast tumor growth. Cancer Research. 2002;62(15):4491-4498.

4. Mathew B, Lennon FE, Siegler J, Mirzapoiazova T, Mambetsariev N, Sammani S, Gerhold LM, LaRiviere PJ, Chen CT, Garcia JG, Salgia R, Moss J, Singleton P. The novel role of the mu opioid receptor in lung cancer progression: a laboratory investigation. Anesthesia & Analgesia. 2011;112(3):558-567.

5. Lennon FE, Moss J, Singleton PA. The μ-opioid receptor in cancer progression: is there a direct effect? Anesthesiology. 2012;116(4):940-945 910.

6. Farooqui M, Li Y, Rogers T, Poonawala T, Griffin RJ, Song CW and Gupta K. COX-2 inhibitor celecoxib prevents chronic morphine-induced promotion of angiogenesis, tumour growth, metastasis and mortality, without compromising analgesia. British Journal of Cancer. 2007;97(11 ):1523 -1531.

7. Zylla D, Gourley BL, Vang D, Jackson S, Boatman S, Lindgren B, Kuskowski MA, Le C, Gupta K, Gupta P. Opioid requirement, opioid receptor expression, and clinical outcomes in patients with advanced prostate cancer. Cancer. 2013;119(23):4103-4110.

8. Lupp A, Richter N, Doll C, Nagel F, Schulz S. UMB-3, a novel rabbit monoclonal antibody, for assessing μ-opioid receptor expression in mouse, rat and human formalin-fixed and paraffin-embedded tissues. Regulatory Peptides. 2011;167(1):9-13.

9. Donahue RN, McLaughlin PJ, Zagon IS. Low-dose naltrexone suppresses ovarian cancer and exhibits enhanced inhibition in combination with cisplatin. Exp Biol Med (Maywood). 2011 Jul;236(7):883-95.

10. Christopherson R, James KE, Tableman M, Marshall P, Johnson FE. Long-term survival after colon cancer surgery: a variation associated with choice of anesthesia. Anesth Analg. 2008;107(1):325-332.