Class G antibodies specific for benzo[a]pyrene, estradiol and progesterone in women with colorectal cancer
https://doi.org/10.21294/1814-4861-2022-21-5-52-58
Abstract
The study was aimed to determine the level of class G antibodies specific to Bp, Es, Pg (IgG-Bp, IgG-Es, IgG-Pg) in patients with colorectal and breast cancers. Material and methods. The content of these antibodies in the blood serum of healthy women (n=401), patients with colorectal cancer (n=219) and patients with breast cancer (n=1469) was studied using a non-competitive enzyme immunoassay. Statistical analysis of the results was performed using the Statistica 8.0 software. Results. The levels of IgG-Bp >7 and IgG-Es>6 were higher in patients with colorectal cancer than in healthy controls (66 % vs 25 %, p<0.0001, OR=5.9 and 58 % vs s 45 %, p=0.002, OR=1.7, respectively). The individual antibody ratios of IgG-Bp/IgG-Es >1, IgG-Bp/IgG-Pg>1.5, and IgG-Es/IgG-Pg>1.5 were also higher in patients with colorectal cancer than in healthy controls (74 % vs 34 %, p<0.0001, OR=5.6; 75 % vs 28 %, p<0.0001, and 58 % vs 38 %, p<0.0001, OR=2.3, respectively). Compared to healthy controls, breast cancer patients had higher values of IgG-Bp >6 (57 % vs 33 %, p<0.0001, OR=2.7) and IgG-Es>5 (62 % vs 53 %, p=0.003, or=1.4) and ratios of IgG-Bp/IgG-Es>1 (55 % vs 34 %, p<0.0001, or=2.4), IgG-Bp/IgG-Pg>1.3 (71 % vs 36 %, p<0.0001, or=4.5) and IgG-Es/IgG-Pg>1.4 (62 % vs 44 %, p<0.0001, or=2.1). Compared to breast cancer patients, colorectal cancer patients had higher values of IgG-Bp>7 (66 % vs 50 %, p<0.0001) and the ratios of igg-Bp/IgG-Es >1 (74 % vs 55 %, p<0.0001) and IgG-Bp/IgG-Pg>1.5 (76 % vs 60 %, p<0.0001). Conclusion. IgG-Bp, IgG-Es, and IgG-Pg immunoassay could serve as a screening tool to identify population at risk of colorectal and breast cancers.
About the Authors
A. V. AverianovRussian Federation
Anton V. Averianov, Leading Engineer-Biologist of the Immunochemistry Laboratory
18, Sovetsky Ave., 650099, Kemerovo, Russia
A. V. Antonov
Russian Federation
Alexander V. Antonov, MD, Head of Department No. 5
35, Volgogradskaya st., 650036, Kemerovo, Russia
A. S. Zhivotovsky
Russian Federation
Alexey S. Zhivotovsky, MD, PhD, Head of Department No. 6
35, Volgogradskaya st., 650036, Kemerovo, Russia
M. V. Kostyanko
Russian Federation
Mikhail V. Kostyanko, Leading Engineer, Department of Organic and Physical Chemistry
6, Krasnaya st., 650000, Kemerovo, Russia
I. A. Vafin
Russian Federation
Ilgiz A. Vafin, MD, Chief Physician
22ak7, Oktyabrsky Ave., 650066, Kemerovo, Russia
G. I. Kolpinskiy
Russian Federation
Gleb I. Kolpinskiy, MD, Head physician
53/1, Oktyabrsky Ave., 650066, Kemerovo, Russia
References
1. Malignant tumors in Russia in 2019 (morbidity and mortality). Ed. by A.D. Kaprin, V.V. Starinsky, A.O. Shakhzadova. Moscow, 2020. 214 p. (in Russian).
2. Khudolei V.V. Carcinogens: characteristics, patterns, mechanisms of action. St. Petersburg, 1990, 419 p. (in Russian).
3. Gunter M.J., Divi R.L., Kulldorff M., Vermeulen R., Haverkos K.J., Kuo M.M., Strickland P., Poirier M.C., Rothman N., Sinha R. Leukocyte polycyclic aromatic hydrocarbon-DNA adduct formation and colorectal adenoma. Carcinogenesis. 2007; 28(7): 1426–9. doi: 10.1093/carcin/bgm022.
4. Jamin E.L., Riu A., Douki T., Debrauwer L., Cravedi J.P., Zalko D., Audebert M. Combined genotoxic effects of a polycyclic aromatic hydrocarbon (B(a)P) and an heterocyclic amine (PhIP) in relation to colorectal carcinogenesis. PLoS One. 2013; 8(3). doi: 10.1371/journal.pone.0058591.
5. Harris D.L., Washington M.K., Hood D.B., Roberts L.J., Ramesh A. Dietary fat-influenced development of colon neoplasia in Apc Min mice exposed to benzo(a)pyrene. Toxicol Pathol. 2009; 37(7): 938–46. doi: 10.1177/0192623309351722.
6. Agudo A., Peluso M., Munnia A., Luján-Barroso L., Barricarte A., Amiano P., Navarro C., Sánchez M.J., Quirós J.R., Ardanaz E., Larrañaga N., Tormo M.J., Chirlaque M.D., Rodríguez-Barranco M., SánchezCantalejo E., Cellai F., Bonet C., Sala N., González C.A. Aromatic DNA adducts and breast cancer risk: a case-cohort study within the EPIC-Spain. Carcinogenesis. 2017; 38(7): 691–8. doi: 10.1093/carcin/bgx047.
7. Santen R.J., Yue W., Wang J.P. Estrogen metabolites and breast cancer. Steroids. 2015; 99(Pt A): 61–6. doi: 10.1016/j.steroids.2014.08.003.
8. Yu F.L. 17Beta-estradiol epoxidation as the molecular basis for breast cancer initiation and prevention. Asia Pac J Clin Nutr. 2002; 11(7): 460–6. doi: 10.1046/j.1440-6047.11.s.7.4.x.
9. Glushkov A.N., Polenok E.G., Gordeeva L.A., Mun S.A., Kostyanko M.V., Antonov A.V., Titov V.A., Verzhbitskaya N.E., Vafin I.A. Immunological imbalance in breast cancer and lung cancer in postmenopausal women. Medical Immunology. 2018; 20(6): 927–34. (in Russian). doi: 10.15789/1563-0625-2018-6-927-934.
10. Glushkov A.N., Polenok E.G., Mun S.A., Gordeeva L.A., Kostyanko M.V., Lutsenko V.A., Kolpinskiy G.I., Brezhneva E.V., Vafin I.A. Immunological phenotype and hormonal balance in postmenopausal women. Russian Journal of Immunology. 2020; 23(1): 61–8. (in Russian). doi: 10.15789/1028-7221-007-IPA.
11. Hajian-Tilaki K. Receiver Operating Characteristic (ROC) Curve Analysis for Medical Diagnostic Test Evaluation. Caspian J Intern Med. 2013; 4(2): 627–35.
12. De Buck S.S., Augustijns P., Muller C.P. Specific antibody modulates absorptive transport and metabolic activation of benzo[a]pyrene across Caco-2 monolayers. J Pharmacol Exp Ther. 2005; 313(2): 640–6. doi: 10.1124/jpet.104.081034.
13. Glushkov A.N., Polenok E.G., Mun S.A., Gordeeva L.A. Inversion of natural immuno-hormonal interactions under influence of antibodies against environmental chemical carcinogens. Med Hypotheses. 2020; 144. doi: 10.1016/j.mehy.2020.109981.
14. Rawlings N.C., Kennedy S.W., Henricks D.M. The active immunization of the cyclic ewe against an estrone protein conjugate. Theriogenology. 1979; 12(3): 139–51. doi: 10.1016/0093-691x(79)90080-3.
15. Hogan A.M., Collins D., Baird A.W., Winter D.C. Estrogen and gastrointestinal malignancy. Mol Cell Endocrinol. 2009; 307(1-2): 19–24. doi: 10.1016/j.mce.2009.03.016.
16. Sasso C.V., Santiano F.E., Campo Verde Arboccó F., Zyla L.E., Semino S.N., Guerrero-Gimenez M.E., Pistone Creydt V., López Fontana C.M., Carón R.W. Estradiol and progesterone regulate proliferation and apoptosis in colon cancer. Endocr Connect. 2019; 8(3): 217–29. doi: 10.1530/EC-18-0374.
Review
For citations:
Averianov A.V., Antonov A.V., Zhivotovsky A.S., Kostyanko M.V., Vafin I.A., Kolpinskiy G.I. Class G antibodies specific for benzo[a]pyrene, estradiol and progesterone in women with colorectal cancer. Siberian journal of oncology. 2022;21(5):52-58. (In Russ.) https://doi.org/10.21294/1814-4861-2022-21-5-52-58