نتایج جستجو برای: tumor associated antigen

تعداد نتایج: 1998750  

Journal: :Oncology reports 2008
Xiu-Min Zhang Yun-Fei Zhang Yang Huang Ping Qu Bin Ma Shao-Yan Si Zeng-Shan Li Wen-Xin Li Xia Li Wei Ge Pei-Zhen Hu Yan-Fang Sui

Tumor antigen-derived peptides have been widely used to elicit tumor-specific cytotoxic T lymphocytes (CTLs). MAGE gene products are of particular interest owing to their wide expression in many tumors and their potential to induce tumor-specific CTL responses. Antigen-specific CTLs induced by MAGE gene-derived peptides have proven to be highly efficacious in the prevention and treatment of var...

Journal: :Cancer research 1979
R A Pattillo M T Story A C Ruckert

A cell-mediated cytotoxicity test, quantitated by postlabeling with tritiated thymidine, was used to asses immune reactivity of cancer patients to the HeW cell line derived from serous cystadenocarcinoma of the ovary. Lymphocytes from 71.4% of serous and mucinous cystadenocarcinoma patients demonstrated a cytotoxic response towards the HeW cells, whereas no reactivity was observed towards targe...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2008
Mala Chakraborty Elizabeth K Wansley Jorge A Carrasquillo Sarah Yu Chang H Paik Kevin Camphausen Michael D Becker William F Goeckeler Jeffrey Schlom James W Hodge

PURPOSE Exposing human tumor cells to sublethal doses of external beam radiation up-regulates expression of tumor antigen and accessory molecules, rendering tumor cells more susceptible to killing by antigen-specific CTLs. This study explored the possibility that exposure to palliative doses of a radiopharmaceutical agent could alter the phenotype of tumor cells to render them more susceptible ...

Journal: :iranian journal of basic medical sciences 0
sheida shariat department of pharmaceutics, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran ali badiee nanotechnology research center, school of pharmacy, mashhad university of medical sciences, mashhad, iran seyed amir jalali department of immunology, medical school, shahid beheshti university of medical sciences, tehran, iran mercedeh mansourian nanotechnology research center, school of pharmacy, mashhad university of medical sciences, mashhad, iran seyed alireza mortazavi department of pharmaceutics, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran mahmoud reza jaafari biotechnology research center, nanotechnology research center, school of pharmacy, mashhad university of medical sciences, mashhad, iran

objective(s):tumor-associated antigen (taa) subunit-based vaccines constitute promising tools for anticancer immunotherapy. however, a major limitation in the development of such vaccines is the poor immunogenicity of peptides when used alone.the aim of this study was to develop an efficient vaccine delivery system and adjuvant to enhance anti-tumor activity of a synthetic her2/neu derived pept...

Journal: :Tumori 2011
Hongjiang Yan Renben Wang Kunli Zhu Wei Zhao Shumei Jiang Rui Feng Xiaoqing Xu Xiangjiao Meng Huiying Sun Haiqin Zhang Dianbin Mu Zhongfa Xu

OBJECTIVES The purpose of the study was to identify predictive factors of tumor response to preoperative chemoradiotherapy for rectal adenocarcinoma. METHODS Ninety-eight patients with nonmetastatic rectal adenocarcinoma received preoperative concurrent chemoradiotherapy and underwent mesorectal excision. After treatment, tumor response according to tumor regression grade were evaluated. The ...

Journal: :Obstetrics and gynecology 2002
Kiyoshi Ohara Yumiko Tanaka Hajime Tsunoda Masato Nishida Shinji Sugahara Yuji Itai

OBJECTIVE To investigate the possibility of objective clinical assessment of the radioresponse of cervical cancer via determination of serum squamous cell carcinoma antigen levels and magnetic resonance imaging (MRI)-based estimation of tumor shrinkage. METHODS The cases of 60 patients undergoing definitive radiotherapy for cervical squamous cell carcinoma (stage I-II: n = 20; stage III-IV: n...

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