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کاربرد نوع شرط:
- جایگاه : پژوهشی
- مجله: Asian Pacific Journal of Cancer Prevention
- نوع مقاله: Journal Article
- کلمات کلیدی: mTOR,estrogen receptor (ER),Progesterone receptor (PgR),Human epidermal growth factor receptor-2 (HER2/neu),Tyrosine kinase
- چکیده:
- چکیده انگلیسی: Objective: To analyze the effect of sirolimus and sunitinib in blocking the tumor growth and to evaluate the expressions of estrogen receptor (ER), progesterone receptor (PgR), and human epidermal growth factor receptor-2 (HER2/neu) after treated with sirolimus and sunitinib. Methods: Thirty-two female Sprague Dawley rats at age 21-days old were administered intraperitoneally with N-Methyl-N-Nitroso Urea (NMU), dosed at 70mg/kg body weight. The rats were divided into 4 groups; Group 1 (Control, n=8), Group 2 (Sirolimus, n=8), Group 3 (Sunitinib, n=8) and Group 4 (Sirolimus+Sunitinib, n=8), being treated twice when the tumor reached the size of 14.5±0.5 mm and subsequently sacrificed after 5 days. The protein expressions of ER, PgR and HER2/neu of the tumor tissues were evaluated by using immunohistochemistry analysis. Results: Treatment with sirolimus alone lowered expressions of ER and PgR of breast cancer and reduced tumor size. There was no significant difference of ER and PgR expressions between control and sunitinib treated tumor. Sunitinib treated tumors reduce in diameter after the first treatment, however the diameter increases after the second treatment. Histologically, sunitinib treated tumor did not show any aggressive invasive carcinoma of no special type (NST) histological subtypes. In addition, all NMU-induced tumors are HER2/neu-negative scoring. Conclusion: Sirolimus is neither synergistic nor additive with sunitinib for breast cancer treatment.
- انتشار مقاله: 13-12-1398
- نویسندگان: Nurul Fathiyatul Nabila Jaffar,Muhammad Shahidan Muhammad Sakri,Hasnan Jaafar,Wan Faiziah Wan Abdul Rahman,Tengku Ahmad Damitri Al-Astani Tengku Din
- مشاهده
- جایگاه : پژوهشی
- مجله: Asian Pacific Journal of Cancer Prevention
- نوع مقاله: Journal Article
- کلمات کلیدی: VEGF,VEGFR-1,VEGFR-2,thyroid nodular hyperplasia,Papillary Thyroid Carcinoma
- چکیده:
- چکیده انگلیسی: Introduction: Vascular endothelial growth factor (VEGF) is an angiogenic factor that plays an important role in
thyroid cancer. VEGF is known to have high affinity to VEGF receptors such as VEGFR-1 (Flt-1) and VEGFR-2 (KDR).
Papillary thyroid carcinoma (PTC) is the most common thyroid cancer and studies showed the increasing incidence of
PTC arising in nodular hyperplasia. Targeted therapy on these growth factors and receptors are used in management
of both differentiated and undifferentiated thyroid carcinoma. This study aims to determine the expression of VEGF
and VEGF receptors (VEGFR) in thyroid nodular hyperplasia and PTC. Methods: A cross-sectional study based on
paraffinized archival tissue blocks of 113 nodular hyperplasias and 67 PTC from the thyroidectomy specimens in
the year of 2003 to 2014. The tissue sections were then stained by immunohistochemistry for VEGF, VEGFR-1 and
VEGFR-2. The lymph node involvement and extrathyroid extension also were determined. Results: The mean age of
PTC patients was 44.7±15.8 years and nodular hyperplasia were 42.2±13.6 years. There was a statistical difference
of VEGFR-1 (p=0.028) and VEGFR-2 (p=0.003) expression between nodular hyperplasia and PTC. However, no
significant difference of VEGF expression (p=0.576) between both diseases. Co-expression of VEGF and VEGFR-1
was significant in both nodular hyperplasia (p=0.016) and PTC (p=0.03), meanwhile no relevant relationship for VEGF
and VEGFR-2 expression (p>0.05). No significant association (p>0.05) between lymph node status and extrathyroid
extension with age groups, gender, VEGF and VEGFR expression. Conclusions: VEGF, VEGFR-1 and VEGFR-2
showed overexpression in both nodular hyperplasia and PTC. The expression of VEGFR-1 and VEGFR-2 are more
significant in PTC with relevant co-expression of VEGF and VEGFR-1. Therefore, the inhibition of VEGFR offers a
promising prospect for tumour management in thyroid carcinoma.- انتشار مقاله: 10-06-1397
- نویسندگان: Nur Hidayati Mohamad Pakarul Razy,Wan Faiziah Wan Abdul Rahman,Thin Thin Win
- مشاهده