جستجوی مقالات مرتبط با کلیدواژه "gene expression level" در نشریات گروه "پزشکی"
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Background
This study aims to analyze the clinicopathological characteristics of breast cancer (BC) patients with different genotypes who underwent radiotherapy. The goal is to explore the relationship between these characteristics and the risk of recurrence, providing valuable insights for clinical adjuvant therapy.
Materials and MethodsA retrospective analysis was conducted on pathological data of 256 BC patients who underwent surgical resection and radiotherapy. Data included age structure, tumor diameter and grading, estrogen receptor (ER) and progesterone receptor (PR) indicators, human epidermal growth factor receptor 2 (HER2), and the cell proliferation antigen marker (Ki-67). Multifactorial analysis was employed to assess correlations.
ResultsThe distribution of BC patients in the low, medium-high, and high-risk groups was 70.9%, 23.2%, and 5.6%, respectively. Multifactorial analysis revealed that PR, Ki-67 expression, and histological grading were independent factors influencing the RS score, with corresponding P values less than 0.05. They were positively correlated (P < 0.001) with Ki-67 expression levels and tumor tissue grading, and negatively correlated with hormonal indicators. The short-term probability of survival for patients with the four staged BC in the low-risk group was 82.34%, 76.12%, 62.13%, and 60.23%, and 23.69%, respectively. Triple negative breast cancer (TNBC) patients and those with Luminal B BC exhibited a higher risk of metastasis (P < 0.05).
ConclusionThe pathological characteristics of BC patients with different genotypes showed significant differences. TNBC patients and those with Luminal B BC should be particularly vigilant about their risk of recurrence and metastasis, and strengthen prognostic considerations.
Keywords: Gene Expression Level, Breast Cancer, Estrogen Receptor, Progesterone Receptor, Recurrence Risk Score -
فصلنامه علوم پزشکی دانشگاه آزاد اسلامی، سال بیست و هفتم شماره 4 (پیاپی 90، زمستان 1396)، صص 244 -251سابقه و هدفکلستاز، به دلیل عدم ورود ترشحات صفراوی به داخل روده کوچک رخ می دهد. در صورت درمان نشدن، کلستاز قادر است آسیب های جدی را به اندام های مختلف بدن وارد کند. همچنین این اختلال می تواند بر بیان ژن های دخیل در آپوپتوز اثرگذار باشد. در این پژوهش، اثرات کلستاز بر تغییرات بیان دو ژن دخیل در آپوپتوز Bad و Bcl-xl در ناحیه استریاتوم مغز رت های نر و نیز تاثیر کورکومین بر بیان ژن ها در این ناحیه از مغز رت ها بررسی شد.روش بررسیدر این مطالعه تجربی، تعداد 16 سر رت به 4 گروه BDL، BDL-کورکومین، شم-کورکومین و کنترل تقسیم شدند. رت های گروه BDL تحت جراحی BDL (انسداد مجاری صفراوی) و گروه BDL-کورکومین، علاوه بر جراحی، تحت تیمار با کورکومین قرار گرفتند؛ درحالی که گروه شم-کورکومین فقط استرس جراحی را دریافت کرده و با دارو تیمار شدند وگروه کنترل هیچ گونه جراحی و تیمار دارویی نداشتند. سپس استریاتوم از مغز رت ها خارج شد و پس از طی مراحل استخراج RNA و سنتز cDNA، سنجش بیان ژن ها مورد بررسی قرار گرفت.یافته هابا توجه به بررسی های به عمل آمده در میزان بیان ژن های پروآپوپتوتیک به آنتی آپوپتوتیک (Bad/Bcl-xl) تفاوت معنی داری بین BDL و BDL-curcumin دیده شد (05/0>p)، اما تفاوت معنی داری بین گروه شم-کورکومین و BDL-کورکومین در سلول های ناحیه استریاتوم مغز رت ها دیده نشد.نتیجه گیریکورکومین باعث کاهش بیان ژن پروآپوتوتیک نسبت به آنتی آپوپتوتیک و باعث کاهش آپوپتوز ناشی از BDL می شود؛ لذا از کورکومین می توان برای کاهش زیان بخش کلستاز استفاده کرد.کلید واژگان: کلستاز, آپوپتوز, تغییرات بیان ژن, کورکومین, استریاتوم, رتMedical Science Journal of Islamic Azad Univesity Tehran Medical Branch, Volume:27 Issue: 4, 2018, PP 244 -251BackgroundCholestasis occurs when the secretion of bile flow into the small intestine is impaired. Without appropriate treatment, cholestasis could induce harmful injuries to different organs. Moreover, this disorder could alter the expression level of apoptotic-related genes. Herein, the effect of cholestasis on the expression level of both anti- and pro-apoptotic genes, Bcl-xl and Bad, in the striatum area of rats were investigated. In addition, we aimed to examine whether curcumin could change the mRNA expression level of aforementioned genes in striatum area of rats.Materials And MethodsIn this experimental study, sixteen male Wistar rats were divided into 4 groups, consisting control, sham-curcumin, BDL and BDL-curcumin groups. Rats in BDL group experienced bile duct obstruction surgery; however, in BDL-curcumin group, rats underwent surgery plus curcumin treatment. Sham-curcumin group were only treated with drug. The control group did not have either surgery or drug treatment. The striatum area of the brain was isolated and after RNA extraction and cDNA synthesis, the expression level of genes were investigated.ResultsThe ratio of pro-apoptotic to anti-apoptotic genes (Bad/Bcl-xl) in the BDL group significantly changed, compared to other groups (pConclusionCurcumin decreased the relative expression level of death promoter to death repressor genes and reduced the BDL-induced apoptosis. Hence, curcumin can be used to reduce the harmful effect of cholestasis.Keywords: Cholestasis, Apoptosis, Gene expression level, Rats, Striatum
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BackgroundAfter radiation therapy (RT), some health hazards including DNA damages may occur where melatonin can play a protective role due to free radical generation. On the other hand, serious accidental overexposures may occur during RT due to nuclear accidents which necessitate the need for study on exposure to high-dose radiations during treatments.ObjectiveThe aim of this study was to study the expression level of two genes in non-homologous end joining (NHEJ) pathways named Xrcc4 and Xrcc6 (Ku70) in order to examine the effect of melatonin on repair of DNA double-strand breaks (BSBs) caused by 8Gy ionizing radiation.MethodsOne hundred eight male Wistar rats were irradiated with a whole body gamma radiation dose of 8Gy with or without melatonin pretreatments. They were divided into six different groups of control, 100 mg/kg melatonin alone, 8Gy irradiation alone, vehicle alone, vehicle plus 8Gy irradiation and 100 mg/kg melatonin plus 8Gy irradiation. Peripheral blood samples were collected at 8, 24 and 48 h after irradiation. Ku70 and Xrcc4 gene expression were evaluated by real-time quantitative polymerase chain reaction (qPCR) technique and analyzed by one-way ANOVA test.ResultsExpression of Ku70 and Xrcc4 genes normalized against Hprt gene showed significant difference in melatonin plus irradiation group at 8h compared to the control group (pConclusionWe concluded that, by increasing expression level of Ku70 and Xrcc4 genes, 100 mg/kg melatonin administration 8 and 24 h before 8 Gyionizing radiation can significantly affect the repair of DNA DSBs in NHEJ pathway.Keywords: Ionizing Radiation, Melatonin, Gene Expression Level, Ku70, Xrcc4
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