Title of article :
OCT-4, an Embryonic Stem Cell Marker Expressed in Breast, Brain and Thyroid Carcinomas Compared to Testicular Carcinoma
Author/Authors :
Madjd, Z Dep Pathology - Iran University of Medical Sciences, Tehran - Cellular Molecular Research Centre - Iran University of Medical Sciences, Tehran - Oncopathology Research Centre - Iran University of Medical Sciences, Tehran - Cancer Research Centre - Shahid Beheshti University of Medical Sciences, Tehran , Hashemi, F Oncopathology Research Centre - Iran University of Medical Sciences, Tehran - Dep Pathology - Iran University of Medical Sciences, Tehran , Shayanfar, N Dep Pathology - Iran University of Medical Sciences, Tehran , Farahani, E Oncopathology Research Centre - Iran University of Medical Sciences, Tehran , Zarnani, AH Nanotechnology Research Center - Avicenna Research Institute - ACECR, Tehran - Immunology Research Center - Iran University of Medical Sciences, Tehran , Sharifi, AM Dep of Pharmacology - Iran University of Medical Sciences, Tehran - Cellular Molecular Research Centre - Iran University of Medical Sciences, Tehran , Akbari, ME Cancer Research Centre - Shahid Beheshti University of Medical Sciences, Tehran
Abstract :
Introduction: Cancer stem cells are a small subpopulation of cells within a tumor
which are responsible for maintaining the tumor mass. A number of factors such as
OCT-4 that govern the fate of adult stem cells also play a role in malignant cell
transformation. OCT-4 is a key regulator of self-renewal in embryonic stem cells; its
expression is potentially correlated with tumorigenesis and can affect some aspects
of tumor behavior such as tumor recurrence or resistance to therapies.
Methods: We have investigated the potential expression of OCT-4 on a panel of
tumors including breast, brain, thyroid and testicular carcinomas, using
immunohistochemistry. The level of expression of OCT-4 was then compared to
different tumor types and degree of differentiation.
Results: OCT-4 was expressed at the highest levels on nuclear site of seminoma
compared with other tumors. The expression of OCT-4 was detectable in both
nucleus and the cytoplasm of almost all breast tumors, but it was detectable at much
lower level in normal breast tissues. OCT-4 expression was noted on poorly
differentiated papillary carcinoma of thyroid compared to normal follicles of
thyroid gland adjacent to the tumor.
Conclusion: Breast carcinomas and papillary carcinomas of thyroid express
elevated levels of embryonic stem cell gene OCT-4, suggesting that these tumors
may contain cells indicative of embryonic-like stem cells. Identification of cancer stem
cells in different malignant tumors may be useful for prognostic evaluation and
administration of a new treatment which target this sub-population of tumor cells.
Keywords :
cancer stem cells , breast cancer , seminoma , oct-4