RU2016133587A - Системы и способы для идентификации злокачественных новообразований, имеющих активированные рецепторы прогестерона - Google Patents

Системы и способы для идентификации злокачественных новообразований, имеющих активированные рецепторы прогестерона Download PDF

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RU2016133587A
RU2016133587A RU2016133587A RU2016133587A RU2016133587A RU 2016133587 A RU2016133587 A RU 2016133587A RU 2016133587 A RU2016133587 A RU 2016133587A RU 2016133587 A RU2016133587 A RU 2016133587A RU 2016133587 A RU2016133587 A RU 2016133587A
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nucleic acid
group
detecting
tissue sample
progesterone receptor
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Кристин Л. КЛАРК
Дж. Динни ГРЭХЭМ
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Дзе Юниверсити Оф Сидней
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    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/74Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving hormones or other non-cytokine intercellular protein regulatory factors such as growth factors, including receptors to hormones and growth factors
    • G01N33/743Steroid hormones
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    • A61K31/337Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
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    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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    • A61K31/573Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone substituted in position 21, e.g. cortisone, dexamethasone, prednisone or aldosterone
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    • A61K31/704Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin attached to a condensed carbocyclic ring system, e.g. sennosides, thiocolchicosides, escin, daunorubicin
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    • A61K31/7064Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
    • A61K31/7068Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
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Claims (25)

1. Способ лечения пациента с использованием антипрогестина, включающий в себя:
получение образца ткани, подозреваемой на туморогенность или злокачественность, от пациента;
обнаружение геномной ДНК, ассоциированной с прогестероновым рецептором в образце ткани;
обнаружение первого уровня транскрипции одной или нескольких ДНК-мишеней, ассоциированных с прогестероновым рецептором, в образце ткани, где ДНК-мишени выбирают из группы, состоящей из T47D2822, T47D299, T47D3514, T47D4414, T47D4818, T47D5045 и T47D5516;
обнаружение второго уровня транскрипции одной или нескольких ДНК-мишеней, ассоциированных с прогестероновым рецептором, в образце ткани с отрицательным контролем, где ДНК-мишени выбирают из группы, состоящей из T47D2822, T47D299, T47D3514, T47D4414, T47D4818, T47D5045 и T47D5516;
сравнение первого и второго уровней транскрипции; и
введение антипрогестина пациенту если уровень транскрипции одной или нескольких ДНК-мишеней, ассоциированных с прогестероновым рецептором, составляет, по меньшей мере, приблизительно в 4 раза выше, чем уровень в образце с отрицательным контролем.
2. Способ по п. 1, где образец ткани выбирают из группы, состоящей из менингиом молочной железы, мозга, сарком простаты, яичника, эндометрия, матки, лейомиомы матки и ткани легкого.
3. Способ по п. 1, где антипрогестин выбирают из группы, состоящей из онапристона, лонаприсана, мифепристона, PF-02413873, телапристона, лилопристона, ORG2058, апоприснила, улипристала, ZM172406, ZM150271, ZM172405 и аглепристона.
4. Способ по п. 1, где антипрогестин вводят пациенту в количестве от приблизительно 10 мг до приблизительно 200 мг в день.
5. Способ по п. 1, дополнительно включающий в себя введение противоопухолевого соединения.
6. Способ по п. 5, где противоопухолевое соединение выбирают из группы, состоящей из эверолимуса, трастузумаб, TM1-D, лекарственных средств против HER2, бевацизумаб, паклитаксела, доцетаксела, таксанов, доксорубицина, липосомального доксорубицина, пегилированного липосомального доксорубицина, антрациклинов, антрацендионов, карбоплатина, цисплатина, 5-ФУ, гемцитабина, циклофосфамида, антиэстрогена, селективных модуляторов эстрогенного рецептора, ингибиторов ароматазы и антиандрогенов.
7. Способ по п. 1, дополнительно включающий в себя обнаружение присутствия мотива связывания кофактора.
8. Способ по п. 7, где мотив связывания кофактора представляет собой FOXA1.
9. Способ по п. 1, где геномную ДНК обнаруживают посредством иммунопреципитации.
10. Способ по п. 9, где иммунопреципитацию проводят, используя моноклональные антитела hPRa6 и hPRa7.
11. Способ по п. 1, где прогестероновый рецептор, ассоциированный с геномной ДНК, обнаруживают посредством иммунопреципитации с первичным антителом против PR.
12. Изолированная по существу нуклеиновая кислота, содержащая нуклеиновую кислоту, выбранную из группы, состоящей из T47D2822, T47D299, T47D3514, T47D4414, T47D4818, T47D5045 и T47D5516.
13. Нуклеиновая кислота по п. 12, где нуклеиновая кислота представляет собой ДНК.
14. Нуклеиновая кислота по п. 12, где нуклеиновая кислота представляет собой РНК.
15. Изолированная по существу нуклеиновая кислота, содержащая нуклеиновую кислоту, комплементарную нуклеиновой кислоте, выбранной из группы, состоящей из T47D2822, T47D299, T47D3514, T47D4414, T47D4818, T47D5045 и T47D5516.
16. Нуклеиновая кислота по п. 15, где нуклеиновая кислота представляет собой ДНК.
17. Нуклеиновая кислота по п. 15, где нуклеиновая кислота представляет собой РНК.
18. Набор, содержащий нуклеиновую кислоту по п. 12, и моноклональные антитела для обнаружения присутствия геномных ДНК-мишеней.
19. Набор по п. 18, в котором моноклональные антитела представляют собой hPRa6 и hPRa7.
RU2016133587A 2014-03-12 2015-03-12 Системы и способы для идентификации злокачественных новообразований, имеющих активированные рецепторы прогестерона RU2016133587A (ru)

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US201461951650P 2014-03-12 2014-03-12
US61/951,650 2014-03-12
PCT/IB2015/000312 WO2015136355A1 (en) 2014-03-12 2015-03-12 Systems and methods for identifying cancers having activated progesterone receptors

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US (1) US20150276767A1 (ru)
EP (1) EP3117013A1 (ru)
JP (1) JP2017510557A (ru)
CN (1) CN106460038A (ru)
AU (1) AU2015228524A1 (ru)
CA (1) CA2939861A1 (ru)
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WO2007078599A2 (en) * 2005-12-16 2007-07-12 The Board Of Trustees Of The Leland Stanford Junior University Functional arrays for high throughput characterization of gene expression regulatory elements
CA2822462A1 (en) * 2010-12-20 2012-06-28 The General Hospital Corporation Polycomb-associated non-coding rnas
RU2014147625A (ru) * 2012-04-27 2016-06-20 Реджентс Оф Зэ Юниверсити Оф Миннесота Прогнозирование рака молочной железы, предсказание подтипа прогестероновых рецепторов и предсказание ответа на лечение антипрогестином на основании генной экспрессии
US20140363425A1 (en) * 2013-03-13 2014-12-11 J. Dinny Graham Systems and methods for identifying cancers having activated progesterone receptors

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