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CURRENT CANCER STEM CELL BIOMARKERS IN TONGUE SQUAMOUS CELL CARCINOMA

Yıl 2018, Cilt: 19 Sayı: 2, 197 - 207, 15.10.2018
https://doi.org/10.23902/trkjnat.368829

Öz

Dil
skuamöz hücreli karsinomu (DSHK) son 5 yılda artan insidans ve mortalite
oranları ile birlikte diğer ağız içi kanserleri arasında en kötü huylu kanser
tipi olarak bilinmektedir. DSHK hastalarının yaşam süreleri sınırlı olduğundan
ve mevcut kemo-radyoterapi yaklaşımlarının başarılı olmamasından dolayı acilen
yeni biyolojik belirteçlere ihtiyaç duyulmaktadır. Diğer solid (katı) tümörlerde
olduğu gibi, DSHK’da da, tümörün başlaması, gelişmesi, yayılması, nüksetmesi ve
kemo-radyoterapiye direnç göstermesi noktasında itici bir güç olarak kabul
edilen “kanser kök hücreleri” (KKH) olarak tanımlanan küçük bir alt popülasyonu
da kapsayan heterojen bir hücre popülasyonuna sahiptir. KKH’nin kanser oluşum
sürecinde nasıl bir katkı yaptıklarının altında yatan moleküler mekanizmalar
tamamen anlaşılamamış olmasına rağmen, bilim insanları ve klinik tedavi
uzmanları DSHK da dâhil olmak üzere kansere karşı mücadelede bu hücreleri
tedavi edici araçlar olarak kullanmayı amaçlamaktadır. Burada, DSHK’daki
potansiyel kanser kök hücrelerinin belirteçlerine ışık tutmak için önemli
bulguları ve en güncel literatürü gözden geçirdik ve derledik. Ayrıca, DSHK
kanser başlangıcı, ilerlemesi, invazyonu ya da metastazı sırasında KKH
biyo-belirteçlerinin olası fonksiyonları özetlenmiştir.

Kaynakça

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CURRENT CANCER STEM CELL BIOMARKERS IN TONGUE SQUAMOUS CELL CARCINOMA

Yıl 2018, Cilt: 19 Sayı: 2, 197 - 207, 15.10.2018
https://doi.org/10.23902/trkjnat.368829

Öz

Tongue squamous cell carcinoma (TSCC) is known to be the most malignant
cancer type amongst other oral cancers with increasing incidence and mortality
rates in the past five years. Since the life expectancy for TSCC patients is
limited and the current chemo-radiotherapy treatments are not curative, novel
biomarkers are urgently needed. As
many other solid tumors, TSCC has a heterogeneous
cancer cell population, which includes a small subpopulation identified as
cancer stem cells (CSCs) that are considered as the driving force for tumor
initiation, development, spread, recurrence, and resistance to
chemo-radiotherapy. Although the underlying molecular mechanisms of how CSCs
are involved in the carcinogenesis are not completely understood, scientists
and clinicians aim to utilize those cells as therapeutic tools in fight against
different cancer types including TSCC. Here, we reviewed and summarized
important findings and the most current literature to shed light on the
potential of cancer stem cells markers in TSCC. Possible functions of CSCs
biomarkers in TSCC pathogenesis during cancer initiation, progression, invasion
or metastasis are also summarized.

Kaynakça

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  • 83. Weng, J., Zhang, H., Wang, C., Liang, J., Chen, G., Li, W., Tang, H. & Hou, J. (2017). miR-373-3p Targets DKK1 to Promote EMT-Induced Metastasis via the Wnt/β-Catenin Pathway in Tongue Squamous Cell Carcinoma. Biomed Research International, 2017: 6010926.
  • 84. Wu, T.F., Chen, L., Bu, L.L., Gao, J., Zhang, W.F. & Jia, J. (2017). CD44+ cancer cell-induced metastasis: A feasible neck metastasis model. European Journal of Pharmaceutical Sciences, 101: 243-250.
  • 85. Xing, Y., Qi, J., Deng, S., Wang, C., Zhang, L. & Chen, J. (2013). Small interfering RNA targeting ILK inhibits metastasis in human tongue cancer cells through repression of epithelial-to-mesenchymal transition. Experimental Cell Research, 319(13): 2058-2072.
  • 86. Yanagisawa, A., Endo, C., Okawa, K., Shitara, S., Kugoh, H., Kakitani, M., Oshimura, M. & Tomizuka, K. (2005). Generation of chromosome-specific monoclonal antibodies using in vitro-differentiated transchromosomic mouse embryonic stem cells. Stem Cells, 23(10): 1479-1488.
  • 87. Yanamoto, S., Yamada, S., Takahashi, H., Naruse, T., Matsushita, Y., Ikeda, H., Shiraishi, T., Seki, S., Fujita, S., Ikeda, T., Asahina, I. & Umeda, M. (2014). Expression of the cancer stem cell markers CD44v6 and ABCG2 in tongue cancer: effect of neoadjuvant chemotherapy on local recurrence. International Journal of Oncology, 44(4): 1153-1162.
  • 88. Yu, X. & Li, Z. (2016). MicroRNA expression and its implications for diagnosis and therapy of tongue squamous cell carcinoma. Journal of Cellular and Molecular Medicine, 20(1): 10-16.
  • 89. Yu, Y.H., Morales, J., Feng, L., Lee, J.J., El-Naggar, A.K. & Vigneswaran, N. (2015). CD147 and Ki-67 overexpression confers poor prognosis in squamous cell carcinoma of oral tongue: a tissue microarray study. Oral Surgery Oral Medicine Oral Pathology Oral Radiology, 119(5): 553-565.
  • 90. Zhang, H. X., Liu, O.S., Deng, C., He, Y., Feng, Y.Q., Ma, J.A., Hu, C.H. & Tang, Z.G. (2017). Genome-wide gene expression profiling of tongue squamous cell carcinoma by RNA-seq. Clinical Oral Investigations, 22(1): 209-216.
  • 91. Zhang, Z., Filho, M.S. & Nör, J.E. (2012). The biology of head and neck cancer stem cells. Oral Oncology, 48(1): 1-9.
  • 92. Zheng, M., Jiang, Y.P., Chen, W., Li, K.D., Liu, X., Gao, S.Y., Feng, H., Wang, S.S., Jiang, J., Ma, X.R., Cen, X., Tang, Y.J., Chen, Y., Lin, Y.F., Tang, Y.L. & Liang, X.H. (2015). Snail and Slug collaborate on EMT and tumor metastasis through miR-101-mediated EZH2 axis in oral tongue squamous cell carcinoma. Oncotarget, 6: 6797-6810.
  • 93. Zou, B., Sun, S., Qi, X. & Ji, P. (2012). Aldehyde dehydrogenase activity is a cancer stem cell marker of tongue squamous cell carcinoma. Molecular Medicine Reports, 5(4): 1116-1120.
Toplam 93 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Yapısal Biyoloji
Bölüm Derleme/Review
Yazarlar

Omer Faruk Karatas

Seyma Teber Bu kişi benim

Ahmet Yilmaz Bu kişi benim

Asli Baltacioglu Bu kişi benim

Selinay Merve Kilic Bu kişi benim

Emel Poyraz Bu kişi benim

Abdulmelik Aytatli Bu kişi benim

Sumeyye Ozturk Bu kişi benim

Ayse Varol Bu kişi benim

Yayımlanma Tarihi 15 Ekim 2018
Gönderilme Tarihi 19 Aralık 2017
Kabul Tarihi 3 Haziran 2018
Yayımlandığı Sayı Yıl 2018 Cilt: 19 Sayı: 2

Kaynak Göster

APA Karatas, O. F., Teber, S., Yilmaz, A., Baltacioglu, A., vd. (2018). CURRENT CANCER STEM CELL BIOMARKERS IN TONGUE SQUAMOUS CELL CARCINOMA. Trakya University Journal of Natural Sciences, 19(2), 197-207. https://doi.org/10.23902/trkjnat.368829
AMA Karatas OF, Teber S, Yilmaz A, Baltacioglu A, Kilic SM, Poyraz E, Aytatli A, Ozturk S, Varol A. CURRENT CANCER STEM CELL BIOMARKERS IN TONGUE SQUAMOUS CELL CARCINOMA. Trakya Univ J Nat Sci. Ekim 2018;19(2):197-207. doi:10.23902/trkjnat.368829
Chicago Karatas, Omer Faruk, Seyma Teber, Ahmet Yilmaz, Asli Baltacioglu, Selinay Merve Kilic, Emel Poyraz, Abdulmelik Aytatli, Sumeyye Ozturk, ve Ayse Varol. “CURRENT CANCER STEM CELL BIOMARKERS IN TONGUE SQUAMOUS CELL CARCINOMA”. Trakya University Journal of Natural Sciences 19, sy. 2 (Ekim 2018): 197-207. https://doi.org/10.23902/trkjnat.368829.
EndNote Karatas OF, Teber S, Yilmaz A, Baltacioglu A, Kilic SM, Poyraz E, Aytatli A, Ozturk S, Varol A (01 Ekim 2018) CURRENT CANCER STEM CELL BIOMARKERS IN TONGUE SQUAMOUS CELL CARCINOMA. Trakya University Journal of Natural Sciences 19 2 197–207.
IEEE O. F. Karatas, “CURRENT CANCER STEM CELL BIOMARKERS IN TONGUE SQUAMOUS CELL CARCINOMA”, Trakya Univ J Nat Sci, c. 19, sy. 2, ss. 197–207, 2018, doi: 10.23902/trkjnat.368829.
ISNAD Karatas, Omer Faruk vd. “CURRENT CANCER STEM CELL BIOMARKERS IN TONGUE SQUAMOUS CELL CARCINOMA”. Trakya University Journal of Natural Sciences 19/2 (Ekim 2018), 197-207. https://doi.org/10.23902/trkjnat.368829.
JAMA Karatas OF, Teber S, Yilmaz A, Baltacioglu A, Kilic SM, Poyraz E, Aytatli A, Ozturk S, Varol A. CURRENT CANCER STEM CELL BIOMARKERS IN TONGUE SQUAMOUS CELL CARCINOMA. Trakya Univ J Nat Sci. 2018;19:197–207.
MLA Karatas, Omer Faruk vd. “CURRENT CANCER STEM CELL BIOMARKERS IN TONGUE SQUAMOUS CELL CARCINOMA”. Trakya University Journal of Natural Sciences, c. 19, sy. 2, 2018, ss. 197-0, doi:10.23902/trkjnat.368829.
Vancouver Karatas OF, Teber S, Yilmaz A, Baltacioglu A, Kilic SM, Poyraz E, Aytatli A, Ozturk S, Varol A. CURRENT CANCER STEM CELL BIOMARKERS IN TONGUE SQUAMOUS CELL CARCINOMA. Trakya Univ J Nat Sci. 2018;19(2):197-20.

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