SIALIC ACID IN THE PRIMARY AND DIFFERENTIAL DIAGNOSIS OF LUNG CANCER
##article.numberofdownloads## 22
##article.numberofviews## 61
PDF (Русский)

Keywords

SALIVA
ENZYMES
AMINOTRANSFERASE
ALKALINE PHOSPHATASE
LACTATE DEHYDROGENASE
LUNG CANCER
А-AMYLASE
GAMMA-GLUTAMYLTRANSPEPTIDASE

How to Cite

Belskaya, L., Kosenok, V., & Массард, Ж. (2017). SIALIC ACID IN THE PRIMARY AND DIFFERENTIAL DIAGNOSIS OF LUNG CANCER. Voprosy Onkologii, 63(6), 926–932. https://doi.org/10.37469/0507-3758-2017-63-6-926-932

Abstract

So far optimization problems for diagnostics and prognostication aids remained relevant for lung cancer as a leader in the structure of cancers. Objective: a search for regularities of changes in the saliva enzyme activity in patients with nonsmall cell lung cancer. In the case-control study, 505 people took part, divided into 2 groups: primary (lung cancer, n=290) and control (conventionally healthy, n=215). All the participants went through a questionnaire survey, saliva biochemical counts, and a histological verification of their diagnosis. The enzyme activity was measured with spectrophotometry. Between-group differences were measured with the nonparametric test. It was shown that in terms of lung cancer, we observe metabolic changes, described with the decreased de Ritis coefficient (p<0.001), as well as the increased activity of alanine aminotransferase (p=0.044), alkaline phosphatase (p=0.008, p=0.049), and а-amylase (p=0.009). We have identified specifics of the change in the enzyme activity depending on a histological type of the tumour. There is the observable increased activity of а-amylase in the saliva in lung adenocarcinoma and neuroendocrine tumours (p<0.001). It was established that the enzyme activity decreases with a regional and distant metastasis independently of histological types of lung cancer.
https://doi.org/10.37469/0507-3758-2017-63-6-926-932
##article.numberofdownloads## 22
##article.numberofviews## 61
PDF (Русский)

References

Бельская Л.В., Косенок В.К., Массард Ж., Завьялов A.А. Состояние показателей липопероксидации и эндогенной интоксикации у больных раком легкого // Вестник РАМН. - 2016. - Т. 71. - № 4. - С. 313-322.

Бельская Л.В., Сарф Е.А., Косенок В.К. Биохимия слюны: методы исследования, методическое пособие. - Омск: Омскбланкиздат, 2015. - 70 с.

Клиническая биохимия. Сборник инструкций. - Новосибирск: ЗАО «Вектор-Бест», 2011. - 132 с.

Петрова Г.В., Каприн А.Д., Грецова О.П., Старинский B.В. Злокачественные новообразования в России. - Москва: МНИОИ им. П.А. Герцена, 2015. - С. 259 -282.

Савченко А.А., Лапешин П.В., Дыхно Ю.А. Зависимость активности метаболических ферментов лимфоцитов крови в клетках здоровой и опухолевой ткани легкого у больных раком легкого // Российский биотерапевти-ческий журнал. - 2004. - Т. 4. - № 3. - С. 70-75.

Савченко А.А., Лапешин П.В., Дыхно Ю.А. Состояние иммунной системы и метаболизм здоровых и опухолевых клеток легочной ткани у больных немелкоклеточным раком легкого в зависимости от мета-стазирования // Российский биотерапевтический журнал. - 2005. - Т. 4. - № 2. - С. 106-112.

Adecola S.A., Popoola O.A., Ogundiran S.M. et al. Is gamma glutamyl transferase a diagnostic marker of prostate disease? // International Journal of Medicine and Biomedical Research. - 2013. - Vol. 2. - № 2. - P. 147-151.

Alberg A.J., Brock M.V., Samet J.M. Epidemiology of lung cancer. Murray and Nadel's Textbook of Respiratory Medicine. - 2016. - Vol. 2. - P. 927-939.

Alexander M., Burbury K. A systematic review of biomarkers for the prediction of thromboembolism in lung cancer - Results, practical issues and proposed strategies for future risk prediction models // Thrombosis Research. - 2016. - Vol. 148. - P. 63-69.

Arunkumar S., Arunkumar J.S., Krishna N.B., Shakunthala G.K. Developments in diagnostic applications of saliva in oral and systemic diseases - A comprehensive review // Journal of Scientific and Innovative Research. - 2014. - Vol. 3. - № 3. - P. 372-387.

Asaduzzaman KM, Tania M, Zhang Dz, et al. Antioxidant enzymes and cancer // Chinese Journal of Cancer Research. - 2010. - Vol. 22. - № 2. - P. 87-92.

Detterbeck FC, Lewis SZ, Diekemper R, Addizzo-Harris DJ, Alberts WM. Diagnosis and management of lung cancer // Chest - 2013. - Vol. 143. - № 5. - P. 7-37.

Dokic-Lisanin M, Pantovic V, Jovanovic Z, Samardzic G, Jurisic V. Values of alkaline phosphatase and their isoenzyme profiles in patients with cancer in respect to bone and liver metastasis // Arch. Oncol. - 2013. - Vol. 21. - № 1. - P. 14-16.

Fentiman I.S., Allen D.S. y-Glutamyl transferase and breast cancer risk // British Journal of cancer. - 2010. - Vol. 103. - P. 90-93.

Grigoleit J-S, Kullmann J.S., Overbeck R., Schedlowski M., Engler H. Salivary а-amylase response to endotoxin administration in humans // Psychoneuroendocrinology. - 2013. - Vol. 38. - P. 1819-1823.

Hertz L., Hertz E. Cataplerotic TCA cycle flux determined as glutamate-sustained oxygen consumption in primary cultures of astrocytes // Neurochemical Int. - 2003. - Vol. 43. - № 4-5. - P. 355-361.

Huijgen H.J., Sanders G., Koster R.W. et al. The clinical value of lactate dehydrogenase in serum: a quantitative review // Eur. Clin. Chem Clin. Biochem. - 1997. - Vol. 35. - № 8. - P. 569-579.

Inomata M., Hayashi R., Tokui K. et al. Lactate dehydrogenase and body mass index are prognostic factors in patients with recurrent small cell lung cancer receiving amrubicin // Tumori. - 2015. - DOI: 10.5301/tj.5000435

Jean J-Ch, Liu Y. Joyce-Brady M. The importance of gam-ma-glutamil transferase in lung glutathione homeostasis and antioxidant defense // Bio Factors. - 2003. - Vol. 17. - P. 161-173.

Jin Yun Y., Rok Kim S. Lactate Dehydrogenase (LDH) as a tumor marker for non-small cell lung cancer // Cancer Research and Treatment. - 2002. - Vol. 34. - № 5. - P. 339-344.

Lenler-Petersen P., Grove A., Brock A., Jelnes R. Alphaamylase in resectable lung cancer // Eur. Respir. J. - 1994. - Vol. 7. - P. 941-945.

Liu J, Duan Y. Saliva: A potential media for disease diagnostics and monitoring // Oral Oncology. - 2012. - Vol. 48. - P. 569-577.

Lopez-Rios F, Sanchez-Arago M, Garcia-Garcia E, et al. Loss of the mitochondrial bioenergetics capacity underlies the glucose avidity of carcinomas // Cancer Res. - 2007. - Vol. 67. - P. 9013-9017.

Lung cancer screening. NCCN Clinical Practice Guidelines in Oncology. 2012.

Maellaro E., Dominici S., Del Bello B., et al. Membrane gamma-glutamyl transpeptidase activity of melanoma cells: effects on cellular H2O2 production, cell surface protein thiol oxidation and NF-kB activation status // Journal of Cell Science. - 2000. - Vol. 13. - P. 2671-2678.

Malathi M., Shrinivas B.R. Relevance of serum alkaline phosphatase as a diagnostic aid in lung pathology // Indian J Physiol Pharmacol. - 2001. - Vol. 45. - № 1. - P. 119-121.

Malathi N., Mythili S., Vasanthi H.R. Salivary Diagnostics: A Brief Review // ISRN Dentistry. - 2014. - Vol. 2014. - P. 158786. - DOI: 10.1155/2014/158786

McCleland M.L., Adler A.S., Deming L., Lee L., Blackwood E.M., Solon M., Tao J., Li L., Shames D., Jackson E., Forrest W.F., Firestein R. Lactate Dehydrogenase B is required for the growth of KRAS-dependent lung adenocarcinoma // Clinical Cancer Research. - 2013. - Vol. 19. - № 4. - P. 773-784.

Miller C.S., Foley J.D., Bailey A.L., et al. Current developments in salivary diagnostics // Biomark Med. - 2010. - Vol. 4. - № 1. - P. 171-189.

Nunes L.A., Mussavira S., Bindhu O.S. Clinical and diagnostic utility of saliva as a non-invasive diagnostic fluid: a systematic review // Biochem Med (Zagreb). - 2015. - Vol. 25. - № 2. - P. 177-192.

Ramya A.S., Uppala D., Majumdar S. et al. Are salivary amylase and pH - prognostic indicators of cancers? // Journal of oral biology and craniofacial research. - 2015. - Vol. 5. - P. 81-85.

Schuurbiers O., Meijer T., Kaanders J., Looijen-Sal-amon M.G. et al. Glucose Metabolism in NSCLC Is Histology-Specific and Diverges the Prognostic Potential of 18FDG-PET for Adenocarcinoma and Squamous Cell Carcinoma // J. Thorac. Oncol. - 2014. - Vol. 9. - P. 1485-1493.

Shipper R.G., Silletti E., Vingerhoeds M.H. Saliva as research material: Biochemical, physicochemical and practical aspects // Archives of oral biology. - 2007. - Vol. 52. - P. 1114-1135.

Siegel R., Ma J., Zou Zh, Jemal Ah. Cancer Statistics // CA Cancer J. Clin. - 2014. - Vol. 64. - № 1. - P. 9-29.

Swinson D.E., Jones J.L., Cox G. et al. Hypoxia-inducible factor-1 alpha in non-small cell lung cancer: relation to growth factor, protease and apoptosis pathways // Int. J. Cancer. - 2004. - Vol. 111. - P. 43-50.

Travis W.D., Brambilla E., Noguchi M. et al. Lung adenocarcinoma classification // J. Thorac. Oncol. - 2011. - Vol. 6. - № 2. - P 244-281.

Turkeli S., Atici A.G., Kayhan S., Yilmaz YA. Analysis of pleural amylase levels in chest disease clinic // Journal of Experimental and Clinic Medicine. - 2013. - Vol. 30. - P. 349-352.

Wang Z-X, Yang L-P, Qiu M-Z et al. Prognostic value of preoperative serum lactate dehydrogenase levels for resectable gastric cancer and prognostic nomograms // Oncotarget. - 2016. - Vol. 26. - № 7. - P. 945-956.

Wasif Saif M., Alexander D., Wicox C.M. Serum alkaline phosphatase level as a prognostic tool in colorectal cancer: a study of 105 patients // The Journal of Applied Research. - 2005. - Vol. 5. - № 1. - P. 88-95.

Whitfield JB. Gamma Glutamil Transferase // Critical Reviews in Clinical Laboratory Sciences. - 2001. - Vol. 38. - № 4. - P. 263-355.

Wong D.T. Salivary Diagnostics. - Wiley-Blackwell. - 2008. - 320 p.

Xu FX, Zhang YL, Liu JJ, Zhang DD, Chen HB. Hypoxic markers in non-small cell lung cancer (NSCLC) // European Review for Medical and Pharmacological Sciences. - 2016. - Vol. 20. - P. 849-852.

Yao F., Zhao T, Zhong C., Zhu J., Zhao H. LDHA is necessary for the tumorigenicity of esophageal squamous cell carcinoma // Tumor Biology. - 2013. - Vol. 34. - P. 25-31.

Zhang J., Zhang L., Pan S. et al. Amylase: sensitive tumor marker for amylase-producing lung adenocarcinoma // J. Thorac. Dis. - 2013. - Vol. 5. - № 4. - P. 167-169.

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

© АННМО «Вопросы онкологии», Copyright (c) 2017