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1.
Arch Endocrinol Metab ; 66(2): 237-246, 2022 Apr 28.
Article in English | MEDLINE | ID: mdl-35420266

ABSTRACT

Objective: Cytological analysis and Bethesda classification of thyroid nodules is the standard method of diagnosing differentiated thyroid carcinoma (DTC). However, even for nodules with a non-malignant cytological diagnosis, there is a not insignificant risk of cancer. There are doubts whether this lack of certainty would influence patient prognosis. Our aim was to compare patients with DTC, classified according to the preoperative cytological diagnosis, regarding their evolution. Methods: A retrospective study was carried out with 108 DTC patients submitted to total thyroidectomy (TT) between 2009 and 2015, divided into three groups according to preoperative cytological diagnosis (Bethesda classification): classes I/II, III/IV, and V/VI. Groups were compared for evolution considering response to treatment at last evaluation as well as time disease free. Statistical analysis used ANOVA, chi squared, and Kaplan-Meier curves with p<0.05 considered significant. Results: Groups differed for time between nodule puncture and TT [in months; V/VI (2.35 ± 2.48) < III/IV (7.32 ± 6.34) < I/II (13.36 ± 8.9); p < 0.0001]. There was no significant difference between groups for evolution at final evaluation (disease free status; classes I/II: 71.4%; classes III/IV: 60%; classes V/VI: 66.6%; p = 0.7433), as well as time disease free (in months; classes I/II: 34.57 ± 25.82; classes III/IV: 38.04 ± 26.66; classes V/VI: 30.84 ± 26.34; p = 0.3841). Conclusion: DTC patients classified according to preoperative cytological diagnosis did not differ for evolution. Although patients with non-malignant cytological diagnoses were submitted to TT later, this did not affect the evolution of the cases.


Subject(s)
Adenocarcinoma , Thyroid Neoplasms , Thyroid Nodule , Biopsy, Fine-Needle/methods , Humans , Retrospective Studies , Thyroid Neoplasms/diagnosis , Thyroid Neoplasms/pathology , Thyroid Neoplasms/surgery , Thyroid Nodule/diagnosis , Thyroid Nodule/pathology , Thyroid Nodule/surgery , Thyroidectomy
2.
Arch. endocrinol. metab. (Online) ; 66(2): 237-246, Apr. 2022. tab, graf
Article in English | LILACS-Express | LILACS | ID: biblio-1374258

ABSTRACT

ABSTRACT Objective: Cytological analysis and Bethesda classification of thyroid nodules is the standard method of diagnosing differentiated thyroid carcinoma (DTC). However, even for nodules with a non-malignant cytological diagnosis, there is a not insignificant risk of cancer. There are doubts whether this lack of certainty would influence patient prognosis. Our aim was to compare patients with DTC, classified according to the preoperative cytological diagnosis, regarding their evolution. Subjects and methods: A retrospective study was carried out with 108 DTC patients submitted to total thyroidectomy (TT) between 2009 and 2015, divided into three groups according to preoperative cytological diagnosis (Bethesda classification): classes I/II, III/IV, and V/VI. Groups were compared for evolution considering response to treatment at last evaluation as well as time disease free. Statistical analysis used ANOVA, chi squared, and Kaplan-Meier curves with p<0.05 considered significant. Results: Groups differed for time between nodule puncture and TT [in months; V/VI (2.35 ± 2.48) < III/IV (7.32 ± 6.34) < I/II (13.36 ± 8.9); p < 0.0001]. There was no significant difference between groups for evolution at final evaluation (disease free status; classes I/II: 71.4%; classes III/IV: 60%; classes V/VI: 66.6%; p = 0.7433), as well as time disease free (in months; classes I/II: 34.57 ± 25.82; classes III/IV: 38.04 ± 26.66; classes V/VI: 30.84 ± 26.34; p = 0.3841). Conclusions: DTC patients classified according to preoperative cytological diagnosis did not differ for evolution. Although patients with non-malignant cytological diagnoses were submitted to TT later, this did not affect the evolution of the cases.

3.
CNS Neurol Disord Drug Targets ; 18(5): 405-412, 2019.
Article in English | MEDLINE | ID: mdl-30868970

ABSTRACT

BACKGROUND: Gliomas are aggressive and resilient tumors. Progression to advanced stages of malignancy, characterized by cell anaplasia, necrosis, and reduced response to conventional surgery or therapeutic adjuvant, are critical challenges in glioma therapy. Relapse of the disease poses a considerable challenge for management. Hence, new compounds are required to improve therapeutic response. As hydrolyzed rutin (HR), a compound modified via rutin deglycosylation, as well as some flavonoids demonstrated antiproliferative effect for glioblastoma, these are considered potential epigenetic drugs. OBJECTIVE: The purpose of this study was to determine the antitumor activity and evaluate the potential for modifying tumor aggressivity of rutin hydrolysates for treating both primary and relapsed glioblastoma. METHODS: The glioblastoma cell line, U251, was used for analyzing cell cycle inhibition and apoptosis and for establishing the GBM mouse model. Mice with GBM were treated with HR to verify antitumor activity. Histological analysis was used to evaluate HR interference in aggressive behavior and glioma grade. Immunohistochemistry, comet assay, and thiobarbituric acid reactive substance (TBARS) values were used to evaluate the mechanism of HR action. RESULTS: HR is an antiproliferative and antitumoral compound that inhibits the cell cycle via a p53- independent pathway. HR reduces tumor growth and aggression, mainly by decreasing mitosis and necrosis rates without genotoxicity, which is suggestive of epigenetic modulation. CONCLUSION: HR possesses antitumor activity and decreases anaplasia in glioblastoma, inhibiting progression to malignant stages of the disease. HR can improve the effectiveness of response to conventional therapy, which has a crucial role in recurrent glioma.


Subject(s)
Anaplasia/complications , Anaplasia/prevention & control , Brain Neoplasms/complications , Brain Neoplasms/drug therapy , Glioblastoma/complications , Glioblastoma/drug therapy , Rutin/pharmacology , Rutin/therapeutic use , Animals , Apoptosis/drug effects , Cell Cycle/drug effects , Cell Line, Tumor , Cell Proliferation/drug effects , Humans , Hydrolysis , Mice , Recurrence , Thiobarbituric Acid Reactive Substances/metabolism
4.
Arch Oral Biol ; 59(3): 268-76, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24581848

ABSTRACT

OBJECTIVE: The aim of this study was to evaluate, in vitro, the role of bFGF in the proliferation and expression of collagen type I and fibronectin of dog bone marrow mesenchymal stem cells (dBMMSCs) in comparison with the expression of the same proteins in dog periodontal fibroblasts (dPLFs). DESIGN: dBMMSCs from the iliac crest were cultivated in Dulbecco's Modified Eagle's Medium (DMEM). Flow cytometry analysis (FCA) was used to characterize dBMMSC. Cells were stimulated with bFGF (1, 5 and 10 ng/mL) after 24 and 48 h. Real time RT-PCR was performed to verify collagen type I and fibronectin expressions. MTT assay was used to confirm cellular proliferation. Statistical analyses were performed (ANOVA and Kruskal-Wallis tests; p<0.05). RESULTS: FCA showed 55.98% of CD34+ and 32.67% of CD90+ after bone marrow aspiration; 3.33% of CD34+ and 33.0% of CD90+ before P1. After P2, 10.54% of dBMMSCs expressed CD90, whereas after P3, this number decreased to 1.58%. dPLFs presented 4.04% of CD90+ and 1.05% of CD34+ after P3. MTT evaluation showed increase in dBMSC proliferation with 5 ng/mL bFGF-stimulus after 24-h. Both collagen I and fibronectin expression were very similar between the two cells groups after 24-h stimulation with 1 ng/mL bFGF concentration. Fibronectin and collagen I expressions were higher after 24-h stimulation with 5 ng/mL bFGF. CONCLUSION: dBMMSCs (1 ng/mL-bFGF stimulus after 24 h) are very similar to dPLFs as regards morphological and immunostaining characteristics, and collagen and/or fibronectin production. The dBMMSCs presented the highest protein expression rates with 5 ng/mL-bFGF stimulus after 24-h.


Subject(s)
Bone Marrow Cells/metabolism , Collagen Type I/metabolism , Fibroblast Growth Factor 2/pharmacology , Fibroblasts/metabolism , Fibronectins/metabolism , Mesenchymal Stem Cells/metabolism , Animals , Cell Proliferation/drug effects , Dogs , Flow Cytometry , In Vitro Techniques , Real-Time Polymerase Chain Reaction , Up-Regulation
5.
J Periodontol ; 82(5): 758-66, 2011 May.
Article in English | MEDLINE | ID: mdl-21054226

ABSTRACT

BACKGROUND: Blood-derived products, platelet-poor plasma (PPP) and platelet-rich plasma (PRP), constitute an approach in the enhancement of tissue healing. PRP has also been used as a scaffold for bone marrow stem cells in tissue engineering. This study evaluates the effect of PPP, calcium chloride-activated PRP (PRP/Ca), calcium chloride- and thrombin-activated PRP (PRP/Thr/Ca), and bone marrow mononuclear cells and PRP/Ca (BMMCs/PRP/Ca) on the healing of replanted dog teeth. METHODS: After 30 minutes of extraction, teeth were replanted with 1) no material (control); 2) PPP; 3) PRP/Ca; 4) PRP/Thr/Ca; or 5) BMMCs/PRP/Ca. Histologic, histomorphometric, and immunohistochemical analysis was assessed 120 days after replantation. Data from histomorphometric analysis were analyzed statistically (analysis of variance, Tukey; P <0.05). Quantitative immunohistochemical analysis was analyzed by Kruskal-Wallis and Dunn post hoc test (P <0.05). RESULTS: Flow cytometry analysis showed 55.98% of CD34(+) and 32.67% of CD90/Thy-1 for BMMCs sample. BMMCs/PRP/Ca presented the largest areas of replacement resorption characterized by osseous ingrowth into cementum (P <0.05), with intense immunomarcation for tartrate-resistant acid phosphatase. The PRP/Ca group also showed areas of replacement resorption with significant immunomarcation for osteopontin. PRP/Thr/Ca presented no replacement resorption. PPP showed areas of inflammatory resorption, with immunomarcation for tartrate-resistant acid phosphatase. CONCLUSIONS: The results suggest that platelets activated with thrombin play an important role in the healing of tissues after tooth replantation. Additional studies are necessary to test other materials, because PRP/Ca did not present an appropriate scaffold for undifferentiated cells in the treatment of avulsed teeth.


Subject(s)
Periodontium/physiology , Tissue Engineering/methods , Tooth Replantation/methods , Acid Phosphatase/analysis , Animals , Antigens, CD34/analysis , Biomarkers/analysis , Bone Marrow Cells/physiology , Bone Resorption/pathology , Calcium Chloride/pharmacology , Coagulants/pharmacology , Collagen Type III/analysis , Dental Cementum/pathology , Dogs , Female , Flow Cytometry , Isoenzymes/analysis , Laminin/analysis , Male , Monocytes/physiology , Osteopontin/analysis , Plasma/physiology , Platelet Activation/drug effects , Platelet-Rich Plasma/physiology , Tartrate-Resistant Acid Phosphatase , Thrombin/pharmacology , Thy-1 Antigens/analysis , Time Factors , Tissue Scaffolds , Wound Healing/physiology
6.
Rev. Odontol. Araçatuba (Impr.) ; 30(1): 15-19, jan.-jun. 2009. ilus
Article in Portuguese | BBO - Dentistry | ID: biblio-856845

ABSTRACT

Paciente do sexo masculino, 26 anos de idade, apresentou-se com uma malformação vascular intra oral que há 8 meses associava-se a dores e sangramento. Ao exame intra-oral, foi possível ver que a lesão estendia-se por sua língua, bochecha, lábios, faringe, parótida e palato mole, unilateralmente a direita. A tomografia computadorizada revelou uma grande massa envolvendo a mucosa jugal e obstruindo parcialmente faringe e laringe. O paciente foi submetido ao tratamento paliativo com agente esclerosante até ser encaminhado para um centro anomalias vasculares. O reconhecimento precoce e o tratamento da malformação vascular intra oral é imprescindível para evitar complicações. As diferenças clínicas entre hemangiomas e malformações vasculares e o tratamento destas anomalias devem ser conhecidos para o sucesso de uma resolução, uma vez que o tratamento para um grupo baseia-se no acompanhamento, sendo que as outras devem ser removidas logo que possível. O uso de terminologia comum para ambos os grupos podem resultar em um plano de tratamento errado o qual é melhor realizado em uma abordagem interdisciplinar, onde as estratégias são planejadas numa base individual


A 26-year-old man presented with an 8-month history of intra oral vascular malformation associated with bleeding and pain. At the intra-oral examination, it was possible to see that the lesion took his tongue, cheek, lips, pharyngeal, parotid, mouth floor and soft palate all to right side. A computed tomography revealed a large mass involving the jugal mucosa and partially obstructing pharynx and larynx. He was subjected to palliative treatment with sclerosant agent until discharged for a vascular anomalies center. Early recognition and treatment of the intra oral vascular malformation is imperative to avoid complications. The clinical differences between hemangiomas and vascular malformations and the management of these disfiguring congenital anomalies must be known for a successful resolution, once that the treatment for one group is based on the follow-up and the other must be removed as soon as it can. The use of common terminology for the both group may result in a wrong management. This is best accomplished in an interdisciplinary setting where treatment strategies are planned on an individual basis


Subject(s)
Humans , Male , Adult , Sclerotherapy , Hemangioma , Vascular Malformations
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