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111 results about "Malignant Neoplasm Treatment" patented technology

Treatments for Malignant Neoplasm (Cancer) include: Treatments depend on the specific type of cancer but some types of treatments are common. Chemotherapy. Radiation therapy. Surgery. Biological therapy (immunotherapy)

Method of modulating ship activity

A method of treating or preventing an immune disorder, such as graft versus host disease, in a subject. The method includes the administering a SHIP1 inhibitor, such as 3α-aminocholestane, to a subject in need of treatment. Thus, SHIP1 inhibitors taught herein represent a novel class of small molecules that have the potential to enhance allogeneic transplantation, boost innate immunity and improve the treatment of hematologic malignancies.
Owner:H LEE MOFFITT CANCER CENT & RES INST INC

Chinese medicine formulation for treating cancer and preparation method thereof

InactiveCN101401915AEase back to normalRelief and return to normal activityAntineoplastic agentsPlant ingredientsSide effectLymphatic Spread
The invention provides a Chinese medicine preparation for treating malignancy and a preparation method thereof. The preparation method comprises the following steps: firstly, pseudo-ginseng, Rhizoma Zedoariae, fritillariae thunbergii, Atractylodes macrocephala, edible tulip and Polyporus umbellate are dried and crushed into fine powder according to certain weight percent; secondly, Tephroseris kirilowii, Scutellaria barbata, Artemisia capillaries, radix astragali and liquorice with certain weight percent are added with water for decoction, a decoction solution is formed and filtered, and filtrate is decompressed and concentrated into condensed ointment; and thirdly, the fine powder and the condensed ointment are uniformly mixed, dried and crushed into fine powder which is then uniformly mixed and added with adequate water, so as to obtain the Chinese medicine preparation for treating the malignancy. The Chinese medicine preparation has obvious treatment effect on malignancy, particularly has obvious effects on preventing post-operation recurrence and metastasis and lightening the toxic side effect of chemicotherapy, is applicable to various cancer patients without untoward reaction and toxic side effect, relieves the symptoms and prolongs the life of the patients. The preparation method has simple technique, can improve the quality of the medicine and effectively improve the clinic treatment effect of the medicine.
Owner:西安国医肿瘤医院

Antigenic polypeptide usable as therapeutic agent for malignant neoplasm

This invention provides a new tumor antigen having an epitope that induces a Th1 cell (a CD4-positive T cell specific to MAGE-A4), and a method of application thereof.Specifically, this invention provides a polypeptide that includes an amino acid sequence having the following characteristic a), b), c), d), e) or f) and has a cytokine-producing activity in a Th cell specific to MAGE-A4:a) An amino acid sequence represented by SEQ ID No: 1 or No: 2;b) An amino acid sequence, wherein one to several tens of any amino acids are added to N terminus and / or C terminus of an amino acid sequence represented by SEQ ID No: 1 or No: 2;c) An amino acid sequence, wherein one to five amino acids from N terminus and / or C terminus of an amino acid sequence represented by SEQ ID No: 1 or No: 2 are deleted;d) An amino acid sequence, wherein one to several amino acid residues of an amino acid sequence represented by SEQ ID No: 1 or No: 2 are substituted and / or deleted;e) An amino acid sequence, wherein one to several tens of any amino acids are added to N terminus and / or C terminus of an amino acid sequence, wherein one to several amino acid residues of an amino acid sequence represented by SEQ ID No: 1 or No: 2 are substituted and / or deleted; andf) An amino acid sequence, wherein one to several amino acid residues are substituted in an amino acid sequence, wherein one to five amino acids from N terminus and / or C terminus of an amino acid sequence represented by SEQ ID No: 1 or No: 2 are deleted.
Owner:HOKKAIDO UNIVERSITY

Ramosetron hydrochloride freeze-dried powder injection and preparation method thereof

The invention discloses a ramosetron hydrochloride freeze-dried powder injection and a preparation method thereof. Under illumination, the solution of the existing ramosetron hydrochloride has poor stability, poordrug effects and high drug adverse effects; and the solids of the existing ramosetron hydrochloride have good stability. Therefore, the ramosetron hydrochloride freeze-dried powder injection improves product stability and safety. A preclinical research shows that an antagonistic activity of ramosetron hydrochloride to 5-HT3 acceptors is stronger and more stable than that of the existing 5-HT3 acceptor antagonist; and ramosetron hydrochloride has stronger effect of treatment on chemotherapeutic drug-caused emesis. Therefore, ramosetron hydrochloride is clinically used for preventing and treating digestive tract symptoms such as nausea and emesis caused by cancer-resistant drugs.
Owner:ZHEJIANG YATAI PHARMA

Rheum emodin double-chain biquaternary ammonium salt with anti-cancer activity and preparation method of rheum emodin double-chain biquaternary ammonium salt

The invention discloses a rheum emodin double-chain biquaternary ammonium salt with the anti-cancer activity and a preparation method of the rheum emodin double-chain biquaternary ammonium salt. The rheum emodin double-chain biquaternary ammonium salt is a mixture of a rheum emodin 1,3-site biquaternary ammonium salt and a rheum emodin 3,8-site biquaternary ammonium salt. The preparation method comprises the following steps: performing Williamson etherification reaction on rheum emodin and p-benzyl bromide in the presence of K2CO3 so as to generate a mixture of 1,3-site dibromomethylbenzyl rheum emodin and 3,8-site dibromomethylbenzyl rheum emodin, and further reacting the dibromomethylbenzyl rheum emodin mixture with tertiary amine so as to obtain the mixture of 1,3-site biquaternary ammonium salt and rheum emodin 3,8-site biquaternary ammonium salt, wherein the two biquaternary ammonium salts are isomerides which cannot be separated on a chromatographic column. The anti-cancer activity evaluation shows that the activity of the rheum emodin double-chain biquaternary ammonium salt disclosed by the invention is higher than that of monoquaternary ammonium salt, and the rheum emodin double-chain biquaternary ammonium salt can be used in a medicine for treating malignant tumor, is particularly applicable to treatment on liver cancer, has a relatively small inhibition effect on normal cells, and has relatively great application prospect.
Owner:FUZHOU UNIV

Therapeutic vaccine for malignant tumors and composition thereof

The invention relates to a therapeutic vaccine for malignant tumors and a composition thereof. The therapeutic vaccine for malignant tumors is a tumor cell line which contains plasmid of antisense nucleic acid of human transforming growth factor beta (TGF-beta2); the therapeutic vaccine composition for malignant tumors comprises the therapeutic vaccine for malignant tumors and an immunopotentiator, and the immunopotentiator is one selected from the group consisting of a Corynebacterium parvum preparation, a non-cell Corynebacterium parvum preparation, a BCG polysaccharide, a nucleic acid preparation, a Nocardia rubra-cell wall skeleton preparation, a group A Streptococcus preparation, a non-cell group A Streptococcus preparation, a Pseudomonas aeruginosa preparation, a non-cell Pseudomonas aeruginosa preparation, a Brucella preparation, a non-cell Brucella preparation, a non-cell Mycobacterium vaccae preparation and a non-cell Mycobacterium smegmatis preparation, preferably the non-cell Corynebacterium parvum preparation; and the malignant tumors include a lung cancer, a liver cancer, a pancreatic cancer, leukemia, lymphoma, an ovarian cancer, a colon cancer, a stomach cancer and a breast cancer.
Owner:熊慧

Dominant sequence of delta 1 chain complementary determining region (CDR) 3 in gamma delta T lymphocytes, and T cell receptor (TCR) transfected cells and application thereof

ActiveCN102532269AImmunoglobulin superfamilyFungiGamma/Delta T-LymphocyteT lymphocyte
The invention discloses a dominant sequence GTM of a delta 1 chain complementary determining region (CDR) 3 in human gastric cancer tissue-derived tumor-infiltrating gamma delta T lymphocytes, a T cell receptor (TCR) containing the sequence, and TCR transfected cells. The amino acid residue sequence of the GTM is shown as SEQ ID NO.1 in a sequence table. Experiments prove that GTM peptide can be specifically combined with tumor cells, tumor tissue and V delta 1 T cell ligand MICA protein; and a J.RT3-T3.5 cell platform for expressing the TCR containing the dominant sequence GTM of the delta 1 chain CDR3 in the human gastric cancer tissue-derived tumor-infiltrating gamma delta T lymphocytes on a J.RT3-T3.5 surface is established by a lentivirus expression system, gamma delta 1 tumor-infiltrating lymphocytes (TIL) and a tumor identifying and killing mechanism thereof are simulated in the cell level, the killing activity of the transfected cells TCR gamma 4 delta 1 on the tumor cells is obviously increased, and the killing effect is TCR-dependent. The invention plays an important role in the development of medicines for treating malignant tumors and the adoptive treatment of malignant tumors, and has wide application prospects.
Owner:THE INST OF BASIC MEDICAL SCI OF CHINESE ACAD OF MEDICAL SCI

Preparation method of mesenchymal stem cell expressing human-derived immune stimulating factor LIGHT and prepared MSC-L cell

The invention discloses a preparation method of a mesenchymal stem cell expressing a human-derived immune stimulating factor LIGHT. The preparation method comprises the following steps that the mesenchymal stem cell is separated and subjected to primary culture and secondary culture; and by building up a retroviral and lentiviral vector pMIGR3-hLIGHT and a pCDHEF-hLIGHT plasmid, a human LIGHT geneis transferred into the mesenchymal stem cell to build up an MSC-L cell, and the MSC-L cell is the mesenchymal stem cell expressing the human-derived immune stimulating factor LIGHT. The invention further relates to the MSC-L cell prepared by adopting the method and application of the MSC-L cell. According to the application of the MSC-L cell, an umbilical cord is adopted as an MSC source, the human LIGHT gene is transferred into the MSC, the LIGHT is transferred into a tumor tissue through the MSC, the MSC modified by the LIGHT can change the tolerance state of a host to a tumor by generating strong antitumor cells and immune reaction of tumor-related mesenchymal cells, and accordingly the tumor is controlled effectively. The mesenchymal stem cell can be prepared on a large scale, and used for treatment of various solid malignant tumors and prevention of cancers.
Owner:上海金坤生物科技有限公司

Drug-loaded stent with ultrasonic intelligent controlled release

InactiveCN102319453AWith ultrasonic intelligent controlled releaseConfirm new roleSurgeryCoatingsHuman bodyAnticarcinogenic Effect
The invention relates to a stent coating with ultrasonic intelligent controlled release and a preparation method and an application thereof. The invention also provides a drug-loaded stent with ultrasonic intelligent controlled release and a preparation method and an application thereof. The advantages of the invention are that: a new stent coating with the effect of ultrasonic intelligent controlled release is successfully constructed and synthesized; ultrasound is first found and confirmed to have control effect on the temperature-sensitive release of loaded drugs; and a new method is provided for future drug intelligent controlled release; a drug-loaded biliary tract stent with ultrasonic intelligent drug controlled release is synthesized, and a possible and feasible treatment means is provided for the treatment of malignant tumors of hollow organs; ultrasound is first found and confirmed to have significant effect on promoting the release of drugs coated by a temperature-sensitive material by changing the spatial structure of the temperature-sensitive material. By using ultrasound, the effect of drug intelligent controlled release at a designated site is achieved; local anticancer effect is brought into play; the toxic and side effect of anticancer drugs on important human tissue is reduced; and high clinical application value is provided.
Owner:XIN HUA HOSPITAL AFFILIATED TO SHANGHAI JIAO TONG UNIV SCHOOL OF MEDICINE
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