RU2017126601A - Способы и композиции для лечения злокачественных опухолей, ассоциированных с мутацией kras - Google Patents
Способы и композиции для лечения злокачественных опухолей, ассоциированных с мутацией kras Download PDFInfo
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- RU2017126601A RU2017126601A RU2017126601A RU2017126601A RU2017126601A RU 2017126601 A RU2017126601 A RU 2017126601A RU 2017126601 A RU2017126601 A RU 2017126601A RU 2017126601 A RU2017126601 A RU 2017126601A RU 2017126601 A RU2017126601 A RU 2017126601A
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- rnai molecules
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- 238000000034 method Methods 0.000 title claims 27
- 206010028980 Neoplasm Diseases 0.000 title claims 5
- 239000000203 mixture Substances 0.000 title claims 3
- 206010069755 K-ras gene mutation Diseases 0.000 title claims 2
- 230000003211 malignant effect Effects 0.000 title 1
- 108091030071 RNAI Proteins 0.000 claims 13
- 230000009368 gene silencing by RNA Effects 0.000 claims 13
- 201000011510 cancer Diseases 0.000 claims 9
- 210000004881 tumor cell Anatomy 0.000 claims 9
- 241000124008 Mammalia Species 0.000 claims 7
- 239000002773 nucleotide Substances 0.000 claims 7
- 125000003729 nucleotide group Chemical group 0.000 claims 7
- 239000008194 pharmaceutical composition Substances 0.000 claims 7
- 102100030708 GTPase KRas Human genes 0.000 claims 5
- 101000584612 Homo sapiens GTPase KRas Proteins 0.000 claims 5
- 230000035772 mutation Effects 0.000 claims 5
- 239000000546 pharmaceutical excipient Substances 0.000 claims 4
- 206010009944 Colon cancer Diseases 0.000 claims 3
- 101150105104 Kras gene Proteins 0.000 claims 3
- 208000010507 Adenocarcinoma of Lung Diseases 0.000 claims 2
- 208000001333 Colorectal Neoplasms Diseases 0.000 claims 2
- 206010039491 Sarcoma Diseases 0.000 claims 2
- 108020004459 Small interfering RNA Proteins 0.000 claims 2
- 230000000692 anti-sense effect Effects 0.000 claims 2
- 201000010983 breast ductal carcinoma Diseases 0.000 claims 2
- 201000010989 colorectal carcinoma Diseases 0.000 claims 2
- 150000002632 lipids Chemical class 0.000 claims 2
- 201000005249 lung adenocarcinoma Diseases 0.000 claims 2
- 208000004707 mucinous cystadenoma Diseases 0.000 claims 2
- 239000002105 nanoparticle Substances 0.000 claims 2
- 210000000277 pancreatic duct Anatomy 0.000 claims 2
- 208000024891 symptom Diseases 0.000 claims 2
- 108091032973 (ribonucleotides)n+m Proteins 0.000 claims 1
- 206010006187 Breast cancer Diseases 0.000 claims 1
- 208000026310 Breast neoplasm Diseases 0.000 claims 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims 1
- 206010061902 Pancreatic neoplasm Diseases 0.000 claims 1
- 108091081021 Sense strand Proteins 0.000 claims 1
- 230000001594 aberrant effect Effects 0.000 claims 1
- 210000003484 anatomy Anatomy 0.000 claims 1
- 210000000481 breast Anatomy 0.000 claims 1
- 201000006230 breast fibrosarcoma Diseases 0.000 claims 1
- 210000004027 cell Anatomy 0.000 claims 1
- 210000001072 colon Anatomy 0.000 claims 1
- 208000029742 colonic neoplasm Diseases 0.000 claims 1
- 230000001934 delay Effects 0.000 claims 1
- 210000000232 gallbladder Anatomy 0.000 claims 1
- 238000001802 infusion Methods 0.000 claims 1
- 238000002347 injection Methods 0.000 claims 1
- 239000007924 injection Substances 0.000 claims 1
- 238000010255 intramuscular injection Methods 0.000 claims 1
- 239000007927 intramuscular injection Substances 0.000 claims 1
- 239000007928 intraperitoneal injection Substances 0.000 claims 1
- 238000010253 intravenous injection Methods 0.000 claims 1
- -1 lipid compounds Chemical class 0.000 claims 1
- 210000004185 liver Anatomy 0.000 claims 1
- 210000004072 lung Anatomy 0.000 claims 1
- 201000005202 lung cancer Diseases 0.000 claims 1
- 208000020816 lung neoplasm Diseases 0.000 claims 1
- 208000015486 malignant pancreatic neoplasm Diseases 0.000 claims 1
- 210000000496 pancreas Anatomy 0.000 claims 1
- 201000002528 pancreatic cancer Diseases 0.000 claims 1
- 208000008443 pancreatic carcinoma Diseases 0.000 claims 1
- 108090000623 proteins and genes Proteins 0.000 claims 1
- 102000004169 proteins and genes Human genes 0.000 claims 1
- 238000010254 subcutaneous injection Methods 0.000 claims 1
- 239000007929 subcutaneous injection Substances 0.000 claims 1
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Claims (33)
1. Фармацевтическая композиция для лечения или терапии опухоли, ассоциированной с мутацией в гене KRAS или со сверхэкспрессией гена KRAS дикого типа, причем композиция содержит молекулы РНКи и фармацевтически приемлемые вспомогательные вещества, где молекулы РНКи содержат нуклеотидную последовательность, соответствующую последовательности-мишени GST-π.
2. Фармацевтическая композиция по п.1, где молекулы РНКи содержат дуплексную область, содержащую нуклеотидную последовательность, соответствующую последовательности-мишени SEQ ID NO: 287.
3. Фармацевтическая композиция по п.1, где молекулы РНКи содержат антисмысловую цепь, содержащую нуклеотидную последовательность, соответствующую SEQ ID NO: 184, и смысловую цепь, содержащую нуклеотидную последовательность, соответствующую SEQ ID NO: 158.
4. Фармацевтическая композиция по п.1, где молекулы РНКи представляют собой киРНК или кшРНК.
5. Фармацевтическая композиция по п.1, где фармацевтически приемлемые вспомогательные вещества включают одно или более липидных соединений.
6. Фармацевтическая композиция по п.1, где фармацевтически приемлемые вспомогательные вещества включают липидные наночастицы.
7. Фармацевтическая композиция по п.1, где фармацевтически приемлемые вспомогательные вещества включают липидные наночастицы, которые инкапсулируют молекулы РНКи.
8. Способ предотвращения, лечения или ослабления одного или более симптомов злокачественной опухоли, ассоциированной с мутацией KRAS у млекопитающего, нуждающегося в этом, причем способ включает:
идентификацию опухолевой клетки у млекопитающего, причем опухолевая клетка содержит, по меньшей мере, одно из следующего: (i) мутацию гена KRAS и (ii) уровень аберрантной экспрессии белка KRAS; и
введение млекопитающему терапевтически эффективного количества композиции, содержащей одну или более молекул РНКи, которые активны в снижении экспрессии GST-π.
9. Способ по п.8, где млекопитающее представляет собой человека, а GST-π представляет собой человеческий GST-π.
10. Способ по п.8, где молекула РНКи представляет собой киРНК или кшРНК.
11. Способ по п.8, где молекулы РНКи содержат дуплексную область, содержащую нуклеотидную последовательность, соответствующую последовательности-мишени SEQ ID NO: 287.
12. Способ по п.8, где молекулы РНКи содержат антисмысловую цепь, содержащую нуклеотидную последовательность, соответствующую SEQ ID NO: 184, и смысловую цепь, содержащую нуклеотидную последовательность, соответствующую SEQ ID NO: 158.
13. Способ по п.8, где молекула РНКи уменьшает экспрессию GST-π у млекопитающего.
14. Способ по п.8, где введение уменьшает экспрессию GST-π у млекопитающего, по меньшей мере, на 5% в течение, по меньшей мере, 5 дней.
15. Способ по п.8, где введение уменьшает объем злокачественной опухоли у млекопитающего, по меньшей мере, на 5% или, по меньшей мере, на 10% или, по меньшей мере, на 20% или, по меньшей мере, на 30% или, по меньшей мере, на 40% или, по меньшей мере, на 50%.
16. Способ по п.8, где способ уменьшает один или более симптомов злокачественной опухоли или задерживает или прекращает прогрессирование злокачественной опухоли.
17. Способ по п.8, где введение уменьшает рост злокачественных опухолевых клеток у объекта.
18. Способ по п.8, где введение уменьшает рост, по меньшей мере, на 2% или, по меньшей мере, на 5% или, по меньшей мере, на 10% или, по меньшей мере, на 15% или, по меньшей мере, на 20% злокачественных опухолевых клеток у объекта.
19. Способ по п.8, где опухолевые клетки содержат повышенный уровень экспрессии белка KRAS дикого типа по сравнению с таковым в нормальной клетке.
20. Способ по п.8, где опухолевая клетка сверхэкспрессирует РНК или белок GST-π дикого типа.
21. Способ по п.8, где опухолевая клетка содержит мутации в белке KRAS в одном или более из остатков 12, 13 и 61.
22. Способ по п.8, где опухолевая клетка содержит мутации в белке KRAS, и опухоль представляет собой злокачественное новообразование, выбранное из рака легких, рака толстой кишки и рака поджелудочной железы.
23. Способ по п.8, где опухолевая клетка содержит мутации в белке KRAS, и опухоль представляет собой саркому, выбранную из группы, состоящей из аденокарциномы легкого, муцинозной аденомы, протоковой карциномы поджелудочной железы и колоректальной карциномы.
24. Способ по п.8, где злокачественная опухоль представляет собой саркому, выбранную из группы, состоящей из аденокарциномы легкого, муцинозной аденомы, протоковой карциномы поджелудочной железы, колоректальной карциномы, рака молочной железы и фибросаркомы.
25. Способ по п.8, где злокачественная опухоль локализована в анатомической области, выбранной из группы, состоящей из легкого, толстой кишки, поджелудочной железы, желчного пузыря, печени, молочной железы и любой их комбинации.
26. Способ по п.8, где введение осуществляют от 1 до 12 раз в день.
27. Способ по п.8, где введение осуществляют в течение 1, 2, 3, 4, 5, 6 или 7 дней.
28. Способ по п.8, где введение осуществляют в течение 1, 2, 3, 4, 5, 6, 8, 10 или 12 недель.
29. Способ по п.8, где введение представляет собой дозу от 0,01 до 2 мг/кг молекул РНКи, по меньшей мере, один раз в день в течение периода до двенадцати недель.
30. Способ по п.8, где введение обеспечивает среднее AUC (0-конец) от 1 до 1000 мкг*мин/мл и среднее значение Cmax от 0,1 до 50 мкг/мл для молекулы GST-π РНКи.
31. Способ по п.8, где введение представляет собой внутривенную инъекцию, внутрикожную инъекцию, подкожную инъекцию, внутримышечную инъекцию, внутрибрюшинную инъекцию, пероральное введение, местное введение, инфузию или ингаляцию.
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Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10264976B2 (en) * | 2014-12-26 | 2019-04-23 | The University Of Akron | Biocompatible flavonoid compounds for organelle and cell imaging |
| ES2789049T3 (es) * | 2014-12-26 | 2020-10-23 | Nitto Denko Corp | Agentes de interferencia de ARN para modulación génica de GST-pi |
| US11045488B2 (en) * | 2014-12-26 | 2021-06-29 | Nitto Denko Corporation | RNA interference agents for GST-π gene modulation |
| US10792299B2 (en) | 2014-12-26 | 2020-10-06 | Nitto Denko Corporation | Methods and compositions for treating malignant tumors associated with kras mutation |
| US20180002702A1 (en) * | 2014-12-26 | 2018-01-04 | Nitto Denko Corporation | Methods and compositions for treating malignant tumors associated with kras mutation |
| ES2828717T3 (es) * | 2015-06-24 | 2021-05-27 | Nitto Denko Corp | Compuestos ionizables y composiciones y usos de los mismos |
| AU2016371624B2 (en) | 2015-12-13 | 2020-08-27 | Nitto Denko Corporation | siRNA structures for high activity and reduced off target |
| CN109477146B (zh) | 2016-05-10 | 2023-09-19 | 国立大学法人东京医科齿科大学 | 炎症促进因子表达抑制剂、其有效成分的筛选方法、对该方法有用的表达盒、诊断药和诊断方法 |
| WO2018151840A2 (en) * | 2017-02-16 | 2018-08-23 | Nitto Denko Corporation | Methods and compositions for treating malignant tumors |
| US11413243B2 (en) * | 2017-11-06 | 2022-08-16 | Nitto Denko Corporation | Fusogenic compounds for delivery of biologically active molecules |
| AU2018364001A1 (en) | 2017-11-09 | 2020-06-25 | National University Corporation Tokyo Medical And Dental University | Inhibitor of the expression of cancer-promoting factors, screening method for active ingredient thereof, expression cassette useful in said method, diagnostic drug, and diagnostic method |
| CN109777798A (zh) * | 2017-11-13 | 2019-05-21 | 深圳华大生命科学研究院 | 一种基于CRISPR技术治疗KRAS突变恶性肿瘤的sgRNA及其应用 |
| JP6952594B2 (ja) * | 2017-12-15 | 2021-10-20 | 洋司郎 新津 | 細胞増殖抑制剤及びそれを含むがんの治療若しくは予防用医薬組成物 |
| CN108486011B (zh) * | 2018-03-27 | 2020-05-05 | 山东大学 | 一种三联苯化合物、制备方法及其应用 |
| JP7432929B2 (ja) * | 2018-05-31 | 2024-02-19 | コリア ユニバーシティ リサーチ アンド ビジネス ファウンデーション | マイクロrnaの非正規標的を抑制するrna干渉誘導核酸およびその用途 |
| WO2020009189A1 (ja) * | 2018-07-05 | 2020-01-09 | 洋司郎 新津 | Braf阻害剤によるがん細胞の逆説的増殖を抑制する薬剤 |
| US20210260095A1 (en) * | 2018-08-22 | 2021-08-26 | Nitto Denko Corporation | Medicine using hsp47 inhibitor to enhance sensitivity to chemotherapeutic agent |
| WO2020040186A1 (ja) | 2018-08-22 | 2020-02-27 | 日東電工株式会社 | Hsp47の阻害物質を用いた、がん転移抑制 |
| PT3880212T (pt) | 2018-11-16 | 2024-02-08 | Nitto Denko Corp | Formulação e métodos de administração de rna de interferência para tumores malignos |
| CN113038956A (zh) * | 2018-12-05 | 2021-06-25 | 日东电工株式会社 | 癌处置用RNAi分子 |
| EP3909588A4 (en) | 2019-01-10 | 2023-01-04 | Osaka University | IMMUNO-STIMULATING COMPOSITION |
| CN113677373A (zh) * | 2019-03-28 | 2021-11-19 | 日东电工株式会社 | RNAi分子 |
| JP2019116507A (ja) * | 2019-04-25 | 2019-07-18 | 有限会社オービット | Hsp47の発現促進剤、脱毛抑制方法、Hsp47の発現促進剤の製造方法及び飲食物の製造方法 |
| JP7463410B2 (ja) * | 2019-07-02 | 2024-04-08 | アルゴノート アールエヌエー リミテッド | アポリポタンパク質bアンタゴニスト |
| US20220267778A1 (en) * | 2019-07-30 | 2022-08-25 | Shionogi & Co., Ltd. | Nucleic acid drug targeting murf1 |
| WO2021146548A1 (en) * | 2020-01-17 | 2021-07-22 | Anastasia Khvorova | Universal dynamic pharmacokinetic-modifying anchors |
| EP4157289A4 (en) | 2020-05-26 | 2024-06-26 | University Of Massachusetts | Synthetic oligonucleotides having regions of block and cluster modifications |
| CN112280800B (zh) * | 2020-10-19 | 2022-06-07 | 上海市东方医院(同济大学附属东方医院) | 一种构建体及其在制备动物衰老细胞示踪和衰老细胞清除药物中的应用 |
| WO2022144882A2 (en) * | 2020-12-28 | 2022-07-07 | 1E Therapeutics, Ltd. | P21 mrna target areas for silencing |
| WO2022144883A2 (en) | 2020-12-28 | 2022-07-07 | 1E Therapeutics, Ltd. | P21 mrna targeting dnazymes |
| KR102732911B1 (ko) * | 2021-12-29 | 2024-11-20 | 의료법인 명지의료재단 | K-ras 특이적 활성화 T 세포를 포함하는 유방암의 예방 및 치료용 약제학적 조성물 및 이의 제조방법 |
| KR102732909B1 (ko) * | 2021-12-29 | 2024-11-20 | 의료법인 명지의료재단 | K-ras 특이적 활성화 T 세포를 포함하는 폐 유두상 선암종의 예방 및 치료용 약제학적 조성물 및 이의 제조방법 |
| KR102732912B1 (ko) * | 2021-12-29 | 2024-11-20 | 의료법인 명지의료재단 | K-ras 특이적 활성화 T 세포를 포함하는 폐 선암종의 예방 및 치료용 약제학적 조성물 및 이의 제조방법 |
| KR102732913B1 (ko) * | 2021-12-29 | 2024-11-20 | 의료법인 명지의료재단 | K-ras 특이적 활성화 T 세포를 포함하는 흑색종의 예방 및 치료용 약제학적 조성물 및 이의 제조방법 |
| KR102732910B1 (ko) * | 2021-12-29 | 2024-11-20 | 의료법인 명지의료재단 | K-ras 특이적 활성화 T 세포를 포함하는 대장암의 예방 및 치료용 약제학적 조성물 및 이의 제조방법 |
| JPWO2023210713A1 (ru) * | 2022-04-27 | 2023-11-02 | ||
| TW202529777A (zh) * | 2023-09-28 | 2025-08-01 | 日商日東電工股份有限公司 | 組合療法 |
Family Cites Families (89)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1989002439A1 (en) | 1987-09-21 | 1989-03-23 | Ml Technology Ventures, L.P. | Non-nucleotide linking reagents for nucleotide probes |
| US5204241A (en) | 1990-10-22 | 1993-04-20 | Oxi-Gene Inc. | Glutathione-S-transferase mu as a measure of drug resistance |
| US5786336A (en) | 1991-04-29 | 1998-07-28 | Terrapin Technologies, Inc. | Target-selective protocols based on mimics |
| US5658780A (en) | 1992-12-07 | 1997-08-19 | Ribozyme Pharmaceuticals, Inc. | Rel a targeted ribozymes |
| DE69431669T2 (de) | 1993-09-02 | 2003-10-23 | Ribozyme Pharmaceuticals, Inc. | Enzymatische nukleiksaüre die nicht-nukleotide enthaltet |
| ES2127948T3 (es) | 1993-10-27 | 1999-05-01 | Ribozyme Pharm Inc | Oligonucleotidos modificados en la posicion 2'-amido y 2'-peptido. |
| EP0831877B1 (en) | 1995-06-07 | 2004-10-27 | Telik, Inc. | Metabolic effects of certain glutathione analogs |
| US5968737A (en) | 1996-11-12 | 1999-10-19 | The University Of Mississippi | Method of identifying inhibitors of glutathione S-transferase (GST) gene expression |
| JPH10330249A (ja) * | 1997-05-30 | 1998-12-15 | Kureha Chem Ind Co Ltd | レチノール化合物含有hsp47合成抑制剤 |
| US6506559B1 (en) | 1997-12-23 | 2003-01-14 | Carnegie Institute Of Washington | Genetic inhibition by double-stranded RNA |
| WO1999054346A1 (en) | 1998-04-16 | 1999-10-28 | Teijin Limited | Glutathione derivatives and dosage forms thereof |
| GB9827152D0 (en) | 1998-07-03 | 1999-02-03 | Devgen Nv | Characterisation of gene function using double stranded rna inhibition |
| DE19956568A1 (de) | 1999-01-30 | 2000-08-17 | Roland Kreutzer | Verfahren und Medikament zur Hemmung der Expression eines vorgegebenen Gens |
| EP1235842A4 (en) | 1999-10-15 | 2003-04-23 | Univ Massachusetts | Rna interference pathway genes as tools for targeted genetic interference |
| GB9927444D0 (en) | 1999-11-19 | 2000-01-19 | Cancer Res Campaign Tech | Inhibiting gene expression |
| WO2005019453A2 (en) | 2001-05-18 | 2005-03-03 | Sirna Therapeutics, Inc. | RNA INTERFERENCE MEDIATED INHIBITION OF GENE EXPRESSION USING CHEMICALLY MODIFIED SHORT INTERFERING NUCLEIC ACID (siNA) |
| US20070083945A1 (en) | 2000-03-10 | 2007-04-12 | Byrum Joseph R | Nucleic acid molecules and other molecules associated with plants |
| WO2001088191A1 (en) | 2000-03-29 | 2001-11-22 | The United States Of America As Represented By The Department Of Veterans Affairs | A novel specific inhibitor of the cyclin kinase inhibitor p21?waf1/cip1¿ |
| JP2004508019A (ja) | 2000-07-28 | 2004-03-18 | コンピュジェン インコーポレイテッド | トランスクリプトームの中に場所を占めるrna転写物及びスプライス変異体を検出するためのオリゴヌクレオチドライブラリー |
| US20040259247A1 (en) | 2000-12-01 | 2004-12-23 | Thomas Tuschl | Rna interference mediating small rna molecules |
| US20030099974A1 (en) | 2001-07-18 | 2003-05-29 | Millennium Pharmaceuticals, Inc. | Novel genes, compositions, kits and methods for identification, assessment, prevention, and therapy of breast cancer |
| US20040142325A1 (en) | 2001-09-14 | 2004-07-22 | Liat Mintz | Methods and systems for annotating biomolecular sequences |
| US20040029275A1 (en) * | 2002-08-10 | 2004-02-12 | David Brown | Methods and compositions for reducing target gene expression using cocktails of siRNAs or constructs expressing siRNAs |
| AU2003295600A1 (en) | 2002-11-14 | 2004-06-15 | Dharmacon, Inc. | Functional and hyperfunctional sirna |
| US20040219600A1 (en) | 2002-12-13 | 2004-11-04 | Williams Robert Wood | Method for determining sensitivity to environmental toxins and susceptibility to parkinson's disease |
| WO2004094636A1 (en) | 2003-04-24 | 2004-11-04 | Galapagos Genomics N.V. | Effective sirna knock-down constructs |
| US20050142596A1 (en) | 2003-11-14 | 2005-06-30 | Krolewski Andrzej S. | Methods of diagnosing renal and cardiovascular disease |
| EP2514758B2 (en) | 2004-03-15 | 2021-06-23 | City of Hope | Methods and compositions for the specific inhibition of gene expression by double-stranded RNA |
| CA2566519C (en) | 2004-05-14 | 2020-04-21 | Rosetta Genomics Ltd. | Micrornas and uses thereof |
| CN101072876B (zh) * | 2004-08-26 | 2012-11-28 | 恩杰内克分子递送有限公司 | 通过细菌性来源的完整小细胞向哺乳动物细胞递送功能性核酸 |
| US9393315B2 (en) * | 2011-06-08 | 2016-07-19 | Nitto Denko Corporation | Compounds for targeting drug delivery and enhancing siRNA activity |
| KR101454286B1 (ko) | 2004-12-22 | 2014-10-27 | 닛토덴코 가부시키가이샤 | 섬유화 억제를 위한 약물 담체 및 약물 담체 키트 |
| CA2605068A1 (en) | 2005-04-15 | 2006-10-26 | The Board Of Regents Of The University Of Texas System | Delivery of sirna by neutral lipid compositions |
| US20070134687A1 (en) * | 2005-09-12 | 2007-06-14 | Aurelium Biopharma Inc. | Focused microarray and methods of diagnosing cancer |
| ES2324128A1 (es) * | 2005-09-29 | 2009-07-30 | Proyecto De Biomedicina Cima, S.L. | Metodo para el diagnostico de carcinoma hepatocelular mediante el empleo de marcadores moleculares. |
| US20090220956A1 (en) * | 2005-10-25 | 2009-09-03 | Dimitry Serge Antoine Nuyten | Prediction of Local Recurrence of Breast Cancer |
| EP2202239A1 (en) | 2005-11-01 | 2010-06-30 | Alnylam Pharmaceuticals Inc. | RNAI inhibition of influenza virus replication |
| RU2448974C2 (ru) * | 2005-11-01 | 2012-04-27 | Элнилэм Фармасьютикалз, Инк. | РНКи-ИНГИБИРОВАНИЕ РЕПЛИКАЦИИ ВИРУСА ГРИППА |
| WO2007051303A1 (en) | 2005-11-02 | 2007-05-10 | Protiva Biotherapeutics, Inc. | MODIFIED siRNA MOLECULES AND USES THEREOF |
| DE602006005084D1 (de) | 2005-11-17 | 2009-03-19 | Childrens Medical Center | Verfahren zur vorhersage und verhinderung der resistenz gegen taxoid-verbindungen |
| US7729737B2 (en) | 2005-11-22 | 2010-06-01 | Isense Corporation | Method and apparatus for background current arrangements for a biosensor |
| US8367628B2 (en) | 2005-12-01 | 2013-02-05 | Pronai Therapeutics, Inc. | Amphoteric liposome formulation |
| US9572886B2 (en) * | 2005-12-22 | 2017-02-21 | Nitto Denko Corporation | Agent for treating myelofibrosis |
| JP5342834B2 (ja) * | 2008-09-05 | 2013-11-13 | 日東電工株式会社 | 骨髄線維症処置剤 |
| WO2007130604A2 (en) * | 2006-05-04 | 2007-11-15 | Baylor Research Institute | Anti-tumor activity of an oncolytic adenovirus-delivered oncogene sirna |
| EP2584047B1 (en) | 2006-05-11 | 2014-11-19 | Alnylam Pharmaceuticals Inc. | Compositions and methods for inhibiting expression of the PCSK9 gene |
| US8067390B2 (en) | 2007-03-02 | 2011-11-29 | The Board Of Regents Of The University Of Texas System | Therapeutic targeting of interleukins using siRNA in neutral liposomes |
| TWI407971B (zh) | 2007-03-30 | 2013-09-11 | Nitto Denko Corp | Cancer cells and tumor-related fibroblasts |
| WO2008124634A1 (en) | 2007-04-04 | 2008-10-16 | Massachusetts Institute Of Technology | Polymer-encapsulated reverse micelles |
| CN101688206B (zh) | 2007-07-05 | 2013-05-15 | 诺瓦提斯公司 | 用于治疗病毒感染的dsRNA |
| EP2193140B1 (en) * | 2007-08-27 | 2016-11-02 | 1Globe Health Institute LLC | Compositions of asymmetric interfering rna and uses thereof |
| WO2009033284A1 (en) | 2007-09-14 | 2009-03-19 | Mcmaster University | Inhibitors of collagen biosynthesis as anti-tumor agents |
| US8372866B2 (en) * | 2008-03-06 | 2013-02-12 | Rottapharm S.P.A. | 2-aryl and 2-heteroaryl 4H-1-benzopyran-4-one-6-amidino derivatives, new pharmacological agents for the treatment of arthritis, cancer and related pain |
| JP2011528910A (ja) * | 2008-07-25 | 2011-12-01 | アルニラム ファーマスーティカルズ インコーポレイテッド | センス鎖中の一般塩基またはミスマッチを使用したsiRNAサイレンシング活性の亢進 |
| CN102159247A (zh) * | 2008-07-30 | 2011-08-17 | 日东电工株式会社 | 药物载体 |
| EP2496700B1 (en) * | 2009-11-04 | 2017-03-01 | The University Of British Columbia | Nucleic acid-containing lipid particles and related methods |
| KR101692063B1 (ko) | 2009-12-09 | 2017-01-03 | 닛토덴코 가부시키가이샤 | hsp47 발현의 조절 |
| US20130053270A1 (en) | 2010-02-24 | 2013-02-28 | Bodysync, Inc. | Methods for determining gene-nutrient interactions |
| US20130004494A1 (en) | 2010-03-12 | 2013-01-03 | Ellen Heber-Katz | Inhibition of P21 and Use Thereof for Inducing Tissue Regeneration |
| US8372819B2 (en) | 2010-04-11 | 2013-02-12 | Salk Institute For Biological Studies | Methods and compositions for targeting skip |
| US8828944B2 (en) | 2010-04-22 | 2014-09-09 | Institut Gustave Roussy | Compounds and uses thereof to induce an immunogenic cancer cell death in a subject |
| AU2011249406B2 (en) | 2010-05-06 | 2015-05-14 | Stem Cell Medicine Ltd. | Stem cell bank for personalized medicine |
| JP5950428B2 (ja) * | 2010-08-05 | 2016-07-13 | 日東電工株式会社 | 線維化組織から正常組織を再生するための組成物 |
| AU2011307259A1 (en) * | 2010-09-30 | 2013-05-02 | Nitto Denko Corporation | Modulation of TIMP1 and TIMP2 expression |
| CN110123830A (zh) | 2010-11-09 | 2019-08-16 | 阿尔尼拉姆医药品有限公司 | 用于抑制Eg5和VEGF基因的表达的脂质配制的组合物和方法 |
| US9011903B2 (en) * | 2011-06-08 | 2015-04-21 | Nitto Denko Corporation | Cationic lipids for therapeutic agent delivery formulations |
| DK2718261T3 (en) | 2011-06-08 | 2016-03-29 | Nitto Denko Corp | Compounds to target drug delivery and promote siRNA activity |
| TWI658830B (zh) | 2011-06-08 | 2019-05-11 | 日東電工股份有限公司 | Hsp47表現調控強化用類視色素脂質體 |
| CN103619355A (zh) * | 2011-06-21 | 2014-03-05 | 日东电工株式会社 | 细胞凋亡诱导剂 |
| CN102896619B (zh) * | 2011-07-26 | 2015-04-22 | 苏州宝时得电动工具有限公司 | 动力工具及其操作方法 |
| GB2507700A (en) * | 2011-08-31 | 2014-05-07 | Alexander A Asea | Compositions and methods for treatment of metastatic cancer |
| US9579338B2 (en) | 2011-11-04 | 2017-02-28 | Nitto Denko Corporation | Method of producing lipid nanoparticles for drug delivery |
| WO2013075140A1 (en) * | 2011-11-17 | 2013-05-23 | The United States Of America, As Represented By The Secretary, Department Of Health & Human Services | Auto -recognizing therapeutic rna/dna chimeric nanoparticles (np) |
| CA2873745A1 (en) * | 2012-05-16 | 2013-11-21 | Aadigen, Llc | Multi-target modulation for treating fibrosis and inflammatory conditions |
| US20140134158A1 (en) | 2012-05-22 | 2014-05-15 | Alberto Bardelli | Kras mutations and resistance to anti-egfr treatment |
| AU2013270685B2 (en) | 2012-06-08 | 2017-11-30 | Nitto Denko Corporation | Lipids for therapeutic agent delivery formulations |
| WO2013192364A1 (en) | 2012-06-22 | 2013-12-27 | The University Of Vermont And State Agricultural College | Treatments of oxidative stress conditions |
| CN104684584A (zh) * | 2012-07-02 | 2015-06-03 | 费卜卢斯坦丁公司 | Gpbp-1的抑制及其治疗用途 |
| US9708607B2 (en) * | 2012-08-03 | 2017-07-18 | Alnylam Pharmaceuticals, Inc. | Modified RNAi agents |
| JP6340162B2 (ja) * | 2012-12-20 | 2018-06-06 | 日東電工株式会社 | アポトーシス誘導剤 |
| KR102255108B1 (ko) | 2013-03-08 | 2021-05-24 | 노파르티스 아게 | 활성제의 전달을 위한 지질 및 지질 조성물 |
| CN103695421B (zh) * | 2013-12-09 | 2016-06-15 | 浙江大学 | 一种特异抑制p21基因表达的siRNA及其应用 |
| US20180002702A1 (en) | 2014-12-26 | 2018-01-04 | Nitto Denko Corporation | Methods and compositions for treating malignant tumors associated with kras mutation |
| CN113559267B (zh) * | 2014-12-26 | 2024-01-12 | 日东电工株式会社 | 细胞死亡诱导试剂、细胞增殖抑制试剂及用于治疗由细胞增殖异常导致的疾病的医药组合物 |
| US20160187319A1 (en) * | 2014-12-26 | 2016-06-30 | Nitto Denko Corporation | Cell death-inducing agent, cell growth-inhibiting agent, and pharmaceutical composition for treatment of disease caused by abnormal cell growth |
| US10264976B2 (en) | 2014-12-26 | 2019-04-23 | The University Of Akron | Biocompatible flavonoid compounds for organelle and cell imaging |
| US10792299B2 (en) * | 2014-12-26 | 2020-10-06 | Nitto Denko Corporation | Methods and compositions for treating malignant tumors associated with kras mutation |
| AU2016371624B2 (en) * | 2015-12-13 | 2020-08-27 | Nitto Denko Corporation | siRNA structures for high activity and reduced off target |
| JP6899201B2 (ja) | 2016-06-23 | 2021-07-07 | 日東電工株式会社 | 細胞死誘導剤、細胞増殖抑制剤及び細胞の増殖異常に起因する疾患の治療用医薬組成物 |
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