Immunohistochemical evaluation of Ki-67, Cyclin D1 and β-catenin expression in the subtypes of triple negative breast cancer

L N Vashchenko , T N Gudtskova , E M Nepomnyashchaya , N S Karnaukhov , M V Kvarchiya

Kazan medical journal ›› 2019, Vol. 100 ›› Issue (2) : 239 -244.

PDF
Kazan medical journal ›› 2019, Vol. 100 ›› Issue (2) : 239 -244. DOI: 10.17816/KMJ2019-239
Experimental medicine
research-article

Immunohistochemical evaluation of Ki-67, Cyclin D1 and β-catenin expression in the subtypes of triple negative breast cancer

Author information +
History +
PDF

Abstract

Aim. To evaluate the expression levels of Ki-67 and cyclin D1 and β-catenin in the subtypes of triple negative breast cancer.

Methods. The study was conducted on the surgical material from 60 patients of clinical stage 2A (T1N1M0 or T2N0M0) who were treated at the Rostov Research Institute of Oncology from 2012 to 2015. For immunohistochemistry, antibodies to estrogen and progesterone receptors, cytokeratins 5/6, Ki-67, cyclin D1, β-catenin, HER2/neu and EGFR proteins were used.

Results. Triple negative breast cancer with the signs of basal epithelium was found to have a significantly higher expression level of Ki-67 compared to non-basal-like one. In some part of triple negative breast cancer samples overexpression of cyclin D1 was observed. The high level of cyclin D1 in the basal-like subtype was less common than in the subtypes without the signs of basal epithelium, but its average value was significantly higher. In triple negative cancer with cyclin D1 overexpression, the loss of β-catenin on the cell membrane and its abnormal accumulation in the cytoplasm was significantly more frequent. β-catenin translocation into the cell nucleus was observed only in basal-like triple negative cancer, and 2 times more often in case of cyclin D1 overexpression.

Conclusion. In triple negative breast cancer tumors with overexpression of cyclin D1 and abnormal expression of β-catenin are observed in some cases; these biomarkers can be considered as potential therapeutic targets for this group of tumors.

Keywords

Ki-67 / triple negative breast cancer / basal-like triple negative breast cancer / Ki-67 / cyclin D1 / β-catenin

Cite this article

Download citation ▾
L N Vashchenko, T N Gudtskova, E M Nepomnyashchaya, N S Karnaukhov, M V Kvarchiya. Immunohistochemical evaluation of Ki-67, Cyclin D1 and β-catenin expression in the subtypes of triple negative breast cancer. Kazan medical journal, 2019, 100(2): 239-244 DOI:10.17816/KMJ2019-239

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Zhukova L.G. Breast cancer with triple-negative phenotype in the Russian population of patients. Clinicalmorphological features. Voprosy onkologii. 2015; 61 (2): 189–194. (In Russ.)

[2]

Жукова Л.Г. Рак молочной железы с тройным негативным фенотипом у российской популяции больных. Клинико-морфологические особенности. Вопр. онкол. 2015; 61 (2): 189-194.

[3]

Brilliant Yu.M., Brilliant A.A., Sazonov S.V. Epithelial cadherins and associated molecules in invasive lobular breast cancer. Arkhiv patologii. 2017; 79 (1): 12–18. (In Russ.)

[4]

Бриллиант Ю.М., Бриллиант А.А., Сазонов С.В. Эпителиальные кадгерины и ассоциированные с ними молекулы при инвазивном дольковом раке молочной железы. Арх. патол. 2017; 79 (1): 12-18. DOI: 10.17116/patol201779112-18.

[5]

Kit O.I., Shatova Yu.S., Frantsiyants E.M. et al. The path to personalized treatment of breast cancer patients. Voprosy onkologii. 2017; 63 (5): 719–723. (In Russ.)

[6]

Кит О.И., Шатова Ю.С., Франциянц Е.М. и др. Путь к персонифицированной тактике лечения больных раком молочной железы. Вопр. онкол. 2017; 63 (5): 719-723.

[7]

Шатова Ю.С., Франциянц Е.М., Новикова И.А. и др. Антиандрогенная терапия: новое направление таргетной терапии рака молочной железы. Соврем. ­пробл. науки и образования. 2017; 3. http://www.science-education.ru/ru/article/view?id=26392 (дата обращения: 07.03.2018). [Shatova Yu.S., Frantsiyants E.M., Novikova I.A. et al. Antiandrogen therapy: a new direction in targeted therapy for breast cancer. Sovremennye problemy nauki i obrazovaniya. 2017; 3. http://www.science-educa

[8]

Шатова Ю.С., Франциянц Е.М., Новикова И.А. и др. Антиандрогенная терапия: новое направление таргетной терапии рака молочной железы. Соврем. пробл. науки и образования. 2017; 3. http://www.science-education.ru/ru/article/view?id=26392 (дата обращения: 07.03.2018).

[9]

tion.ru/ru/article/view?id=26392 (access date: 07.03.2018). (In Russ.)]

[10]

Yanjiao He, Zhaoxia Liu, Chao Qiao et al. Expression and significance of Wnt signaling components and their target genes in breast carcinoma. Molecular Med. Reports. Published online on: 2013: 137-143. DOI: 10.3892/mmr.2013.1774.

[11]

Yanjiao He, Zhaoxia Liu, Chao Qiao et al. Expression and significance of Wnt signaling components and their target genes in breast carcinoma. Molecular Med. Reports. Published online on: 2013: 137–143. DOI: 10.3892/mmr.2013.1774.

[12]

Скворцов В.А., Манихас Г.М. Циклин D1 и его прогностическая значимость в планировании эндокринной терапии у женщин постменопаузального возраста при раке молочной железы. Врач-аспирант. 2012; 50 (1.3): 401-407.

[13]

Skvortsov V.A., Manikhas G.M. Cyclin D1 and its prognostic value in planning of endocrine therapy of women of postmenopousal age with breast cancer. Vrach-aspirant. 2012; 50 (1.3): 401–407. (In Russ.)

[14]

Zhuo W., Zhang L., Wang Y. et al. Cyclin D1 G870A polymorphism is a risk factor for esophageal cancer among Asians. Cancer Invest. 2012; 30 (9): 630-636. DOI: 10.3109/07357907.2012.726385.

[15]

Zhuo W., Zhang L., Wang Y. et al. Cyclin D1 G870A polymorphism is a risk factor for esophageal cancer among Asians. Cancer Invest. 2012; 30 (9): 630–636. DOI: 10.3109/07357907.2012.726385.

[16]

Gayatri R., Anuradha A. Cyclin D1 expression in ductal carcinoma of the breast and its correlation with other prognostic parameters. J. Can. Res. Therap. 2014; 10 (3): 671-675. DOI: 10.4103/0973-1482.138135.

[17]

Gayatri R., Anuradha A. Cyclin D1 expression in ductal carcinoma of the breast and its correlation with ­other prognostic parameters. J. Can. Res. Therap. 2014; 10 (3): 671–675. DOI: 10.4103/0973-1482.138135.

[18]

Pestell R.G. New roles of Cyclin D1. Am. J. Pathol. 2013; 183 (1): 3-9. DOI: 10.1016/j.ajpath.2013.03.001.

[19]

Pestell R.G. New roles of Cyclin D1. Am. J. Pathol. 2013; 183 (1): 3–9. DOI: 10.1016/j.ajpath.2013.03.001.

[20]

Mohammadizadeh F., Hani M., Ranaee M., Bagheri M. Role of cyclin D1 in breast carcinoma. J. Res. Med. Sci. 2013; 18 (12): 1021-1025. PMID: 24523791.

[21]

Mohammadizadeh F., Hani M., Ranaee M., Baghe­ri M. Role of cyclin D1 in breast carcinoma. J. Res. Med. Sci. 2013; 18 (12): 1021–1025. PMID: 24523791.

[22]

Татарский В.В. Сигнальный путь WNT: перспективы фармакологического регулирования. Успехи молекулярн. онкол. 2016; 3 (1): 28-31. DOI: 10.17650/2313-805X-2016-3-1-28-31.

[23]

Tatarskiy V.V. The Wnt signaling pathway: prospects for pharmacological regulation. Uspehi molekularnoj onkologii. 2016; 3 (1): 28–31. (In Russ.)

[24]

Prosperi J.R., Goss K.H. A Wnt-ow of opportunity: targeting the Wnt/beta-catenin pathway in breast cancer. J. Curr. Drug. Targets. 2010; 11: 1074-1088. DOI: 10.2174/138945010792006780.

[25]

Prosperi J.R., Goss K.H. A Wnt-ow of opportunity: targeting the Wnt/beta-catenin pathway in breast cancer. J. Curr. Drug. Targets. 2010; 11: 1074–1088. DOI: 10.2174/138945010792006780.

[26]

Xu J., Prosperi J.R., Choudhury N. et al. β-Catenin is required for the tumorigenic behavior of triple-negative breast cancer cells. PLoS One. 2015; 10 (2): e0117097. DOI: 10.1371/journal.pone.0117097.

[27]

Xu J., Prosperi J.R., Choudhury N. et al. β-Catenin is required for the tumorigenic behavior of triple-negative breast cancer cells. PLoS One. 2015; 10 (2): e0117097. DOI: 10.1371/journal.pone.0117097.

[28]

Артамонова Е.В. Палбоциклиб в комбинации с гормонотерапией при люминальном HER2-негативном метастатическом раке молочной железы: новая высокоэффективная стратегия лекарственного лечения. Опухоли женской репродуктивной системы. 2017; 13 (3): 28-40. DOI: 10.17650/1994-4098-2017-13-3-28-41.

[29]

Artamonova E.V. Palbociclib in combination with hormone therapy for luminal HER2-negative metastatic breast cancer: new highly effective strategy of drug treatment. Opukholi zhenskoy reproduktivnoy sistemy. 2017; 13 (3): 28–40. (In Russ.)

RIGHTS & PERMISSIONS

Vashchenko L.N., Gudtskova T.N., Nepomnyashchaya E.M., Karnaukhov N.S., Kvarchiya M.V.

AI Summary AI Mindmap
PDF

118

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/