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Case Report | DOI: https://doi.org/10.31579/2640-1053/070
1* Department of Medical Biology, Faculty of Medicine, Çukurova University, 01330 Balcalı-Adana, Turkey.
2 Department of Medical Biology, Faculty of Medicine, Adıyaman University, Adıyaman, Turkey.
*Corresponding Author: Osman Demirhan, Department of Medical Biology, Faculty of Medicine, Çukurova University, and 01330 Balcalı-Adana, Turkey, GMS: 05060229765
Citation: Osman Demirhan, Deniz Taştemir Korkmaz, Nesrin Çetinel;Cytogenetic differences in blood and cancer tissue samples of the same patient group; J Cancer Research and Cellular Therapeutics;3(1);DOI: 10.31579/2640-1053/070
Copyright: © 2020, Osman Demirhan: This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Received: 23 July 2020 | Accepted: 31 July 2020 | Published: 07 August 2020
Keywords: breast cancer, chromosomal aberrations, anöploidy, blood tissue, cancer tissue
Breast cancer (BC) is the most prevalent malignant disease in females worldwide. Genomic instability in tumor tissue has been associated with tumor progression. These genetic changes may take a variety of forms, including numerical and structural chromosomal abnormalities (CAs), epigenetic changes, and gene expression alterations. Many tumor tissues are made up of genetically different cell populations, and the study of the causes and consequences of this heterogeneity play a central role in cancer research. In this study, CAs in blood and cancer tissues of patients with sporadic BC were examined. Our findings shows that the increase in numerical sex aneuploidy in BC tissues is significantly higher than in blood tissue. These aneuploidy increases in cancer tissues seem to be compatible with the development and increase of cancer, and can play a role in the pathogenesis of cancers. These changes are consistent with early and long-standing exposure to carcinogens, especially estrogens. These findings should clarify our understanding of breast carcinogenesis in breast tissues and promote development of improved methods for risk assessment and BC prevention in women.
Breast cancer is a major global health problem and the incidence of the disease continues to increase steadily. Sporadic BC develops through the accumulation of genetic abnormalities in normal breast tissue, resulting from exposure to estrogens and other carcinogens beginning at adolescence and continuing throughout life. Technical advances in the field of cancer cytogenetics have greatly enhanced the detection ability of CAs, and have facilitated the research and diagnostic potential of chromosomal studies in neoplasms. Cytogenetic and molecular genetic date are of paramount importance in the diagnosis, prognosis, and risk stratification of patients with malignant diseases. Diagnosis of disease-specific genetic abnormalities can provide the information necessary to assist the oncologist in diagnosing. The DNA in every cell is essentially identical to every other cell. Karyotyping of cancer cells is considered the gold standard method considering that abnormalities in the genome of a single cell are similar to all body cells. Therefore, blood and tissue cells are expected to be genetically matched. Technical advances in the field of cancer cytogenetics, chromosome analysis of a single cell is still the easiest way to delineate and understand the relationship between clonal evolution and disease progression of cancer cells. Therefore, the vast majority of genetic samples used in large-scale studies come in the form of blood. But, there are questions about genetic research based only on blood samples. Because, it is suggested that the genetic damage in blood and tissue cells is different in the same person. CAs are one of the hallmarks of neoplastic cells in general, and the persistent presence of chromosome instability has been demonstrated in many human cancers. Breast carcinomas are among the most heterogeneous human neoplasms. There is more than one genetic damage in the development of malignant BC. These aberrations range from single nucleotide point mutations to structural CAs and gross changes in chromosome copy number. BC progression is characterized by the accumulation of numeric changes on many chromosomes, particularly frequent increases in the copy numbers of chromosomes. Sex chromosome aneuploidy increase was reported to be very high in sarcoma tumor tissue (specifically, polysomies) and in blood tissue, respectively (p<0>
Technical advances in the field of cancer cytogenetics have facilitated the research and diagnostic potential of chromosomal studies in neoplasms. In two studies, in two different patient groups, blood tissues of 51 patients and cancer tissue of 49 breast cancer patients were reffered to Department of Medical Biology and Genetics, Faculty of Medicine, Çukurova University for chromosomal analysis. This study was approved by the Ethics Committee of Medical Faculty, Çukurova University. The blood samples were 51 women with BC, to evaluate these women at retrospectively. The average age of the patientswas 44.6 years (between 10 and 80 years). Metaphase chromosome preparations from peripheral blood tissues were made by the standard cytogenetic protocols. In the other group, 49 fresh cancer tissues were analyzed by FISH method. Cancer tissue biopsies were taken by the Department of General Surgery of Çukurova University Faculty of Medicine with mastectomy. Also, the blood tissues of 32 healty age and sex-matched controls were made by the standard cytogenetic protocols (the mean age 29,44 ± 5,003, ranged 21-38). For the purpose of the study, we used CEP X Spectrum Orange DNA Probe Kit (Abbott). FISH was applied according to the method mentioned by Taştemir et al. (2011) [2]. An average of 500 interphase cells was analyzed using a BX51 Olympus fluorescence microscope equipped with Cytovision Probe Software (Applied Imaging, Santa Clara, CA). Monosomic and polysomic cells for X chromosome positive cells were recorded. Also, cytogenetic analysis of blood samples were conducted by Giemsa-banding and reported according to the current international standard nomenclature (ISCN, 2009) [3].
We evaluated cytogenetic abnormalities in blood and cancer tissues of total 100 histopathologically confirmed BC patients, and 32 females as control. Blood samples of 51 patients was conducted by Giemsa-banding. The karyotype results were abnormal in 31,4% of all patients. Structural and numerical CAs were observed in 27,5% and 3,9% of patients, respectively. Specifically, the deletions and fragilities were the most common karyotypes (7,8%). Translocations were detected in 2% and the frequency of other CAs was 5,9% of the patients. Aneuploidies detected in 3,9% of the patients. The 7p11, 7q32, 9p32, 11p15, 11q12, 11q23, 21q11, 21q21, 15p11 and 17q23 regions were the most common chromosome damage observed in patients. These regions can be play an important role in the development of BC and requires further molecular analysis as a potential candidate region for the isolation of genes related to carcinogenesis. In another patient group, we examined only sex chromosome numerical aberrations in 49 cancer tissues by FISH. There were many X chromosome losses and gains in tumor tissue cells. At least one X chromosome loss (monosomy)/gain (polysomy) was recorded in 35.68% of the cells examined. X chromosome polysomies were categorized as 3X, 4X, 5X, 6X, 7X and 8X and above. It was found that age was effective on total X polysomy and there was a statistical difference between the groups (p = 0.020). It was observed that total X polysomies increased especially due to increasing age and the highest rate was at the age of 71 and over. This difference is mainly due to the increase of 4X cells found statistically significant between the groups (p = 0.012). At the same time, it was observed that the rate of X monosomies was higher in the early stages (I and II) than in the advanced stage (III and IV) and the difference was statistically significant (p=0,020).
Comparisons between groups were applied using The Mann-Whitney U-test and Kruskal-Wallis test were used to compare date that were not normally distributed. The categorical variables between groups were analyzed using the χ2 test. Results are presented as the mean ± standard deviation and the median (range). P<0>
Cancer is known to result from a combination of the genetic defects. Also, the tumors display very complex structural CAs the origin of which are often very difficult to estsablish. The identification of recurrent chromosomal changes is a useful strategy for understanding tumorigenesis and specific chromosomal associations. Tumour cells frequently have structural alterations of chromosomes, including deletions, duplications, inversions and translocations. Most frequently, a loss of genetic material in the form of deletions and the other structural CAs also can be observed in BC patients [1]. However, aneuploidy is also features of cancers that are usually associated with poor prognosis. This study investigates the frequency of chromosomal gains and losses in blood and cancer tissues in BC patients. We reported that numerical sex CAs in cancer tissues were higher than blood tissues and the difference was statistically significant (p<0>
may have an important role in early stage of carcinogenesis in BC patients, and the autosomal aneuploidies play a role in the pathogenesis of BC, and can be used as indicators of malignancies. Several studies have also shown that anöploidies in different chromosomes are associated with aggressive tumor behavior [4,5]. Chromosomal instability could accelerate the rate of loss of heterozygosity of a tumour suppressor gene and/or effectively amplify an oncogene by duplicating the chromosome on which it lies, thus contributing to tumorigenesis.
In the present study, the incidence of all aneuploidies in patients' blood tissues was about 4%, while only one X chromosome loss (monosomy) / gain (polysomy) in the examined cancer tissue cells was found to be 36%. And, the frequencies of sex chromosome aneuploidies were higher in the tumoral tissues than in the blood (p<0>
X chromosome aberrations have been found in the neoplasms of different organs. This shows that the presence of numerical aberrations of the X chromosome indicates that it may play an important role in BC development. Because, aneuploidy and chromosomal instability are features of cancers that are usually associated with poor prognosis, or a cause or consequence of cancer, and it is known to participate in the progression of the disease. However, sex chromosome aneuploidies may therefore offer substantial help in differentiating between non-neoplastic and malignant conditions, may also help to differentiate between benign and malignant lesions. These our observations suggest that the response to aneuploidy might very well be tissue specific. Thus, aneuploidy has a direct effect on the prognosis of patients suffering from breast cancer, and regardless of other parameters we can say that it can be an indicator of poor prognosis.
However, we were also observed that the rate of X monosomia was higher in the early stages of cancer (I and II) than in the advanced stages (III and IV) and the difference was statistically significant (p=0.020). This result shows that aneuploidy is significantly high in the early stages of cancer, and genetic damage is a trigger cause at the beginning of cancer. A distinction between neoplasia and non-neoplastic conditions is based on the presence or absence of clonal chromosome damage. Whereas nonneoplastic lesions were thought to have a normal karyotype, the finding of a clonal abnormality would signify neoplasia. However, it was reported in findings that are not compatible with this. For example, clonal chromosome changes
were found to be significantly different in normal oral mucosa samples in head and neck cancer patients and healthy individuals [8]. However, these clonal CAs in non-neoplastic tissues have been suggested as exemplary exceptions. Why karyotypes may represent cell clone(s) of the tumor has been extensively discussed in the literatures. A most likely explanation is that the malignant cell clones have a growth advantage. It is also possible that some of the abnormal karyotypes may be due to mitoses of malignant cells, because such aberrations are often found in malignant breast lesions.
The loss and gain of the X chromosome in women with aging is much more frequent than that of the Y chromosome in males. However, paradoxically, X chromosome aneuploidy is rarely seen in the dividing cells of the bone marrow in females [9]. A loss of the Y chromosome is frequently observed in myeloproliferative diseases and myelodysplastic syndromes, and can also be seen in lymphoproliferative disorders such as lymphomas [10]. A loss of the Y chromosome in contrast, is a common secondary change in both cancer cells and in a few leukemias. At the same time, the advanced age (71 years and above) was effectived in increasing the total X polysomia in our patients. These findings show that the significantly higher frequency of aneuploidy seen in older ages increases the genomic instability during the progression of the disease. On the other hand, it has been also reported that sex chromosome anöploidies increase with rised age [11]. However, it is known that gender CAs increase with increasing age in lymphocyte cultures of healthy people. Conversely, other studies have shown that age is not clearly related and the X chromosome that are lost reappeared after therapy and during clinical remission. Therefore, it supports the hypothesis that the loss of sex chromosome is due to the evolution of a malignant clone. However, polysomy X was also known to be associated with the tumor stage, with a possible correlation with the degree of tumor.
As a result; the cytogenetics karyotyping and FISH should all be considered to obtain accurate diagnoses of malignancies, especially cancer. This highlights the clinical importance of a combined modality approach for the accurate diagnosis and classifi cation of cancers. It seems that to derive sufficient conclusions for the clinical significance of CAs in BC and to correlate genetic changes with disease, it is necessary that many more cases be studied and that in each case, as many chromosomes or chromosomal regions as possible be evaluated. Our findings show that blood tissue and cancer tissue should be analyzed together for the exact diagnosis, treatment and development of the disease. If possible, the study of fresh cancer tissue should be preferred.
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