Establishment of Doxorubicin Resistant Stem-like Cell line from MCF-7 Cells

{"title":"Establishment of Doxorubicin Resistant Stem-like Cell line from MCF-7 Cells","authors":"","doi":"10.37184/lnjcc.2789-0112.3.14","DOIUrl":null,"url":null,"abstract":"Background\nConventional therapy of Breast cancer (BCa) is associated with numerous challenges, relapse being the topmost. It has been shown that disease relapse occurs due to the existence of cancer stem cells (CSCs), residing within the tumor. \nObjectives\nTo develop a cancer stem cell line model, exploiting the property of stem cells to resist treatment with anti-cancer therapeutic agents and to develop novel therapeutic interventions targeting the elimination of CSCs.\nMethods\nSingle-cell clones (SCC) from MCF-7 cells were established in 96-well plates using a culture medium containing 5% FBS. Enrichment of cancer stem cells was carried out from established single cell clones which were initially cultured in a serum-deprived nutrient medium for six weeks followed by Doxorubicin treatment. Doxorubicin-resistant clones were established and evaluated for their growth and sphere-forming abilities. Further, these clones were characterized based on the presence of stem-cell markers using a semi-quantitative reverse transcription-polymerase chain reaction and results were compared with the parental MCF-7 cell line.\nResults \nIn a complete medium, these spheres differentiated and started growing as a monolayer with differential expression levels of genes involved in stemness and cellular differentiation. When these spheres were sub-cultured again in stem-cell medium and detached to give rise to single cells, these clones retained sphere-forming ability. Doxorubicin-resistant clones showed a tendency to grow in spheres in a stem-cell medium with serum-deprived culture conditions.\nConclusion\nOur results provide undeviating evidence of the successful establishment of clones of MCF-7 cell line exhibiting stem cell-like properties. These cell lines have been reprogrammed as stem cell-like models and can be used to delineate recurrent breast cancer attributed to CSCs.","PeriodicalId":363682,"journal":{"name":"Liaquat National Journal of Cancer Care","volume":"37 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Liaquat National Journal of Cancer Care","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.37184/lnjcc.2789-0112.3.14","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

Background Conventional therapy of Breast cancer (BCa) is associated with numerous challenges, relapse being the topmost. It has been shown that disease relapse occurs due to the existence of cancer stem cells (CSCs), residing within the tumor. Objectives To develop a cancer stem cell line model, exploiting the property of stem cells to resist treatment with anti-cancer therapeutic agents and to develop novel therapeutic interventions targeting the elimination of CSCs. Methods Single-cell clones (SCC) from MCF-7 cells were established in 96-well plates using a culture medium containing 5% FBS. Enrichment of cancer stem cells was carried out from established single cell clones which were initially cultured in a serum-deprived nutrient medium for six weeks followed by Doxorubicin treatment. Doxorubicin-resistant clones were established and evaluated for their growth and sphere-forming abilities. Further, these clones were characterized based on the presence of stem-cell markers using a semi-quantitative reverse transcription-polymerase chain reaction and results were compared with the parental MCF-7 cell line. Results In a complete medium, these spheres differentiated and started growing as a monolayer with differential expression levels of genes involved in stemness and cellular differentiation. When these spheres were sub-cultured again in stem-cell medium and detached to give rise to single cells, these clones retained sphere-forming ability. Doxorubicin-resistant clones showed a tendency to grow in spheres in a stem-cell medium with serum-deprived culture conditions. Conclusion Our results provide undeviating evidence of the successful establishment of clones of MCF-7 cell line exhibiting stem cell-like properties. These cell lines have been reprogrammed as stem cell-like models and can be used to delineate recurrent breast cancer attributed to CSCs.
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MCF-7细胞抗阿霉素干细胞样细胞系的建立
背景:乳腺癌(BCa)的常规治疗与许多挑战相关,复发是最重要的。研究表明,肿瘤复发是由于肿瘤内存在肿瘤干细胞(CSCs)。目的建立肿瘤干细胞系模型,利用干细胞抵抗抗癌药物治疗的特性,开发新的靶向消除CSCs的治疗干预措施。方法采用含5%胎牛血清的培养基,在96孔板上培养MCF-7细胞单细胞克隆。肿瘤干细胞的富集是从已建立的单细胞克隆中进行的,这些单细胞克隆最初在无血清的营养培养基中培养6周,然后用阿霉素治疗。建立了耐多柔比星克隆,并对其生长和成球能力进行了评价。此外,利用半定量逆转录聚合酶链反应对这些克隆进行了干细胞标记的鉴定,并将结果与亲本MCF-7细胞系进行了比较。结果在完整的培养基中,这些球分化并开始生长为单层,与干性和细胞分化相关的基因表达水平存在差异。当这些球体在干细胞培养基中再次传代培养并分离产生单细胞时,这些克隆保留了球体形成能力。阿霉素耐药克隆在无血清培养条件下的干细胞培养基中表现出球形生长的趋势。结论成功建立了具有干细胞样特性的MCF-7细胞系。这些细胞系已被重新编程为干细胞样模型,可用于描述由csc引起的复发性乳腺癌。
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