نمایش مختصر رکورد

dc.contributor.authorNakhjavani, Maryamen_US
dc.contributor.authornikounezhad, nastaranen_US
dc.contributor.authorAshtarinezhad, Azadehen_US
dc.contributor.authorHosseini Shirazi, Farshaden_US
dc.date.accessioned1399-07-09T06:58:35Zfa_IR
dc.date.accessioned2020-09-30T06:58:35Z
dc.date.available1399-07-09T06:58:35Zfa_IR
dc.date.available2020-09-30T06:58:35Z
dc.date.issued2016-11-01en_US
dc.date.issued1395-08-11fa_IR
dc.date.submitted2015-06-20en_US
dc.date.submitted1394-03-30fa_IR
dc.identifier.citationNakhjavani, Maryam, nikounezhad, nastaran, Ashtarinezhad, Azadeh, Hosseini Shirazi, Farshad. (2016). Human Lung Carcinoma Reaction against Metabolic Serum Deficiency Stress. Iranian Journal of Pharmaceutical Research, 15(4), 817-823. doi: 10.22037/ijpr.2016.1940en_US
dc.identifier.issn1735-0328
dc.identifier.issn1726-6890
dc.identifier.urihttps://dx.doi.org/10.22037/ijpr.2016.1940
dc.identifier.urihttp://ijpr.sbmu.ac.ir/article_1940.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/313099
dc.description.abstractCancer treatment is still of the greatest challenges that health care providers and patients are facing. One of the unsolved problems in cancer treatment is cells' reaction to metabolic stress caused by harsh nutritional conditions around tumor. In order to be able to treat this disease properly, it is important to understand the true nature of the disease. In fact, the cells inside the central part of the tumorlack sufficient access to blood vessels, nutrients, and growth signals. After tumor shrinkage, the cells are exposed to favorable environmental conditions and might regrow and cause tumor recurrence. The main purpose of this study was to investigate the effect of serum starvation, as a type of metabolic stress, on human lung cancer cell line, A549. These cells were treated with 10% (control), 0.5% and 0.25% serum for 1 to 5 days. At 24-hour intervals, the cells were released with 10% serum supplemented media. Starved or released cells were studied for their cycle and morphology. The results showed that the cells were actually arrested at G1 phase and following exposure to optimal conditions, the cells could be back to their cycle again. Furthermore, sub-G1 apoptotic cells population was not increased within the starvation period, while control cells had significant increase in sub-G1 cells. Morphological studies also showed that starved cells could make denser colonies while control cells were entering death phase. These observations provide some evidence for the generation of some effective resistance phenomena in cancer cells against harsh metabolic conditions.en_US
dc.format.extent912
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherSchool of Pharmacy, Shahid Beheshti University of Medical Sciencesen_US
dc.relation.ispartofIranian Journal of Pharmaceutical Researchen_US
dc.relation.isversionofhttps://dx.doi.org/10.22037/ijpr.2016.1940
dc.subjectA549en_US
dc.subjectSerumen_US
dc.subjectStarvationen_US
dc.subjectCell Cycleen_US
dc.subjectMetabolicen_US
dc.subjectStressen_US
dc.subjecttoxicology and Pharmacologyen_US
dc.titleHuman Lung Carcinoma Reaction against Metabolic Serum Deficiency Stressen_US
dc.typeTexten_US
dc.typeResearch articleen_US
dc.contributor.departmentDepartment of Pharmaco/Toxicology, School of Pharmacy, Shahid Beheshti Medical University, Tehran, Iran.en_US
dc.contributor.departmentDepartment of Pharmaco/Toxicology, School of Pharmacy, Shahid Beheshti Medical University, Tehran, Iran.en_US
dc.contributor.departmentDepartment of Occupational Hygiene, School of Hygiene, Iran University of Medical Sciences, Tehran, Iran. Occupational Health Research Center, School of Public Health, Iran University of Medical Sciences, Tehran, Iran.en_US
dc.contributor.departmentDepartment of Pharmaco/Toxicology, School of Pharmacy, Shahid Beheshti Medical University, Tehran, Iran. Pharmaceutical Sciences Research Center, Shahid Beheshti Medical University, Tehran, Iran.en_US
dc.citation.volume15
dc.citation.issue4
dc.citation.spage817
dc.citation.epage823


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