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1.
Food Funct ; 8(1): 151-166, 2017 Jan 25.
Article in English | MEDLINE | ID: mdl-27924972

ABSTRACT

The previous study evaluated the antitumor activity and the underlying mechanism of the purified polyphenols from pinecones of Pinus koraiensis (PPP-40) using a tumor-bearing S180 mice model. This study was designed to evaluate the protective effects of PPP-40 on spleen tissues of S180 mice in vivo. Pretreatment with PPP-40 (150 mg per kg BW per D) could significantly inhibit tumor growth, enhance spleen index and prevent the decline of haematological parameters of S180 mice induced by the tumor microenvironment. Moreover, the treatment with PPP-40 was shown to significantly inhibit splenocyte apoptosis by TUNEL staining and flow cytometry, characterized by the inhibition of splenocyte cycle (G0/G1) arrest, increase in the percentages of splenic T lymphocytes (CD3+ T cells) and T cell subsets (CD3+CD4+ and CD3+CD8+ T cells), as well as the production of T cell-related cytokines (IL-2, IL-12, and TNF-α) in splenocytes exposed to the tumor microenvironment. These effects were associated with a decrease in oxidative stress, as evidenced by the changes in the SOD, GSH-Px, GSH and MDA levels of liver and spleen tissues of S180 mice. Furthermore, the protective effect of PPP-40 on spleen tissues was deeply analyzed by detecting apoptosis-related proteins using immunohistochemistry staining. The results indicated that the protective multi-mechanisms of action also were associated with the inhibition of apoptosis through down-regulation protein expressions of Bax, caspase-9, caspase-8 caspase-3, Fas and up-regulation of the expressions of Bcl-2. These results suggested that PPP-40 is a natural antitumor agent and possesses strong immunomodulatory activities by protecting the spleen tissues of tumor-bearing S180 mice.


Subject(s)
Antineoplastic Agents, Phytogenic/administration & dosage , Pinus/chemistry , Plant Extracts/administration & dosage , Polyphenols/administration & dosage , Protective Agents/administration & dosage , Splenic Neoplasms/prevention & control , Animals , Apoptosis/drug effects , Caspases/genetics , Caspases/metabolism , Cell Cycle/drug effects , Cell Line, Tumor , Humans , Interleukin-12/genetics , Interleukin-12/metabolism , Interleukin-2/genetics , Interleukin-2/metabolism , Male , Mice , Oxidative Stress/drug effects , Splenic Neoplasms/genetics , Splenic Neoplasms/metabolism , Splenic Neoplasms/physiopathology , T-Lymphocytes/drug effects , T-Lymphocytes/metabolism , Tumor Burden/drug effects , Tumor Necrosis Factor-alpha/genetics , Tumor Necrosis Factor-alpha/metabolism
2.
Blood ; 100(5): 1648-54, 2002 Sep 01.
Article in English | MEDLINE | ID: mdl-12176884

ABSTRACT

A precise description of clinical features at presentation and analysis of clinical and biologic prognostic factors in splenic marginal zone lymphoma (SMZL) are still lacking. Here we describe the clinical and biologic features of a series of 60 SMZL patients diagnosed after splenectomy. Analysis for overall survival (OS), failure-free survival (FFS), and the probability of obtaining a response was performed using univariate and multivariate tests. The median age of the patient was 63 years (range, 35-84 years). Performance status according to the Eastern Cooperative Oncology Group (ECOG scale) was 0 = 16%, 1 = 58%, and 2 = 25%. Of the 60 patients, 53 (86.6%) were at Ann Arbor stage IV. All 60 patients received splenectomies, 29 of 60 also received chemotherapy, and 2 received spleen radiotherapy. A complete response (CR) was achieved by 38.3% of patients, and a partial response (PR) was achieved by 55%. Mean OS of the series was 103 months (range, 2-164 months); mean FFS was 40 months (range, 3-164 months). At 5 years from diagnosis, 39 patients (65%) were alive. Patients dying from the disease had a relatively aggressive clinical course, with a short survival (17.5 months [range, 2-72 months]). Significant prognostic factors in multivariate analysis were (1) (for OS and FFS) lack of response to therapy (CR versus noncomplete response [nCR]) and involvement of nonhematopoietic sites, and (2) (for the probability of obtaining CR) bone marrow involvement. Chemotherapy did not influence OS or FFS. p53 overexpression predicted a shorter OS in the univariate analysis. These data confirm the relative indolence of this disease, indicating the existence of a subset of more aggressive cases, which should stimulate the search for predictive biologic factors and alternative therapies.


Subject(s)
Lymphoma, B-Cell , Splenic Neoplasms , Adult , Aged , Aged, 80 and over , Analysis of Variance , Disease-Free Survival , Female , Humans , Lymphoma, B-Cell/mortality , Lymphoma, B-Cell/pathology , Lymphoma, B-Cell/physiopathology , Lymphoma, B-Cell/therapy , Male , Middle Aged , Multivariate Analysis , Prognosis , Splenic Neoplasms/mortality , Splenic Neoplasms/pathology , Splenic Neoplasms/physiopathology , Splenic Neoplasms/therapy , Survival Analysis
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