JP2015504847A5 - - Google Patents
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- JP2015504847A5 JP2015504847A5 JP2014544946A JP2014544946A JP2015504847A5 JP 2015504847 A5 JP2015504847 A5 JP 2015504847A5 JP 2014544946 A JP2014544946 A JP 2014544946A JP 2014544946 A JP2014544946 A JP 2014544946A JP 2015504847 A5 JP2015504847 A5 JP 2015504847A5
- Authority
- JP
- Japan
- Prior art keywords
- mir
- cancer
- seq
- metastatic
- mirna
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000002679 microRNA Substances 0.000 claims description 61
- 230000010473 stable expression Effects 0.000 claims description 54
- 108091070501 miRNA Proteins 0.000 claims description 53
- 230000014509 gene expression Effects 0.000 claims description 46
- 230000001965 increasing effect Effects 0.000 claims description 46
- 238000000034 method Methods 0.000 claims description 45
- 230000003247 decreasing effect Effects 0.000 claims description 44
- 238000012360 testing method Methods 0.000 claims description 40
- 239000002246 antineoplastic agent Substances 0.000 claims description 38
- 108091059964 miR-154 stem-loop Proteins 0.000 claims description 32
- 108091039097 miR-193b stem-loop Proteins 0.000 claims description 32
- 108091079015 miR-379 Proteins 0.000 claims description 32
- 108091086215 miR-379 stem-loop Proteins 0.000 claims description 32
- 108091028761 miR-409 stem-loop Proteins 0.000 claims description 32
- 206010028980 Neoplasm Diseases 0.000 claims description 31
- 201000011510 cancer Diseases 0.000 claims description 31
- 230000004043 responsiveness Effects 0.000 claims description 30
- 239000012472 biological sample Substances 0.000 claims description 28
- 229940041181 antineoplastic drug Drugs 0.000 claims description 24
- 150000001875 compounds Chemical class 0.000 claims description 24
- 229940079593 drug Drugs 0.000 claims description 22
- 239000003814 drug Substances 0.000 claims description 22
- 239000003112 inhibitor Substances 0.000 claims description 20
- 206010027476 Metastases Diseases 0.000 claims description 18
- 230000009401 metastasis Effects 0.000 claims description 18
- 229940121358 tyrosine kinase inhibitor Drugs 0.000 claims description 18
- 239000005483 tyrosine kinase inhibitor Substances 0.000 claims description 18
- 150000004917 tyrosine kinase inhibitor derivatives Chemical group 0.000 claims description 18
- 206010061289 metastatic neoplasm Diseases 0.000 claims description 17
- 206010006187 Breast cancer Diseases 0.000 claims description 14
- 206010055113 Breast cancer metastatic Diseases 0.000 claims description 14
- 208000026310 Breast neoplasm Diseases 0.000 claims description 14
- 206010050017 Lung cancer metastatic Diseases 0.000 claims description 14
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims description 14
- 206010060862 Prostate cancer Diseases 0.000 claims description 14
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims description 14
- 210000000988 bone and bone Anatomy 0.000 claims description 14
- 201000005202 lung cancer Diseases 0.000 claims description 14
- 208000020816 lung neoplasm Diseases 0.000 claims description 14
- 208000037819 metastatic cancer Diseases 0.000 claims description 14
- 208000011575 metastatic malignant neoplasm Diseases 0.000 claims description 14
- 208000010658 metastatic prostate carcinoma Diseases 0.000 claims description 14
- 229960004378 nintedanib Drugs 0.000 claims description 12
- XZXHXSATPCNXJR-ZIADKAODSA-N nintedanib Chemical compound O=C1NC2=CC(C(=O)OC)=CC=C2\C1=C(C=1C=CC=CC=1)\NC(C=C1)=CC=C1N(C)C(=O)CN1CCN(C)CC1 XZXHXSATPCNXJR-ZIADKAODSA-N 0.000 claims description 12
- 230000000683 nonmetastatic effect Effects 0.000 claims description 12
- FWMNVWWHGCHHJJ-SKKKGAJSSA-N 4-amino-1-[(2r)-6-amino-2-[[(2r)-2-[[(2r)-2-[[(2r)-2-amino-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]piperidine-4-carboxylic acid Chemical compound C([C@H](C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N1CCC(N)(CC1)C(O)=O)NC(=O)[C@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 FWMNVWWHGCHHJJ-SKKKGAJSSA-N 0.000 claims description 8
- 239000000523 sample Substances 0.000 claims description 8
- 230000001394 metastastic effect Effects 0.000 claims description 7
- 239000005411 L01XE02 - Gefitinib Substances 0.000 claims description 6
- 239000005551 L01XE03 - Erlotinib Substances 0.000 claims description 6
- 239000002176 L01XE26 - Cabozantinib Substances 0.000 claims description 6
- 239000000556 agonist Substances 0.000 claims description 6
- 229960003982 apatinib Drugs 0.000 claims description 6
- 229960001292 cabozantinib Drugs 0.000 claims description 6
- ONIQOQHATWINJY-UHFFFAOYSA-N cabozantinib Chemical compound C=12C=C(OC)C(OC)=CC2=NC=CC=1OC(C=C1)=CC=C1NC(=O)C1(C(=O)NC=2C=CC(F)=CC=2)CC1 ONIQOQHATWINJY-UHFFFAOYSA-N 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 229960001433 erlotinib Drugs 0.000 claims description 6
- AAKJLRGGTJKAMG-UHFFFAOYSA-N erlotinib Chemical compound C=12C=C(OCCOC)C(OCCOC)=CC2=NC=NC=1NC1=CC=CC(C#C)=C1 AAKJLRGGTJKAMG-UHFFFAOYSA-N 0.000 claims description 6
- 229960002584 gefitinib Drugs 0.000 claims description 6
- XGALLCVXEZPNRQ-UHFFFAOYSA-N gefitinib Chemical compound C=12C=C(OCCCN3CCOCC3)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 XGALLCVXEZPNRQ-UHFFFAOYSA-N 0.000 claims description 6
- WPEWQEMJFLWMLV-UHFFFAOYSA-N n-[4-(1-cyanocyclopentyl)phenyl]-2-(pyridin-4-ylmethylamino)pyridine-3-carboxamide Chemical compound C=1C=CN=C(NCC=2C=CN=CC=2)C=1C(=O)NC(C=C1)=CC=C1C1(C#N)CCCC1 WPEWQEMJFLWMLV-UHFFFAOYSA-N 0.000 claims description 6
- 238000011282 treatment Methods 0.000 claims description 6
- IPDMWUNUULAXLU-UHFFFAOYSA-N 3-hydroxy-1-methoxy-9,10-dioxo-2-anthracenecarboxaldehyde Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=C(O)C(C=O)=C2OC IPDMWUNUULAXLU-UHFFFAOYSA-N 0.000 claims description 4
- 239000005462 Mubritinib Substances 0.000 claims description 4
- -1 batalanib Chemical compound 0.000 claims description 4
- 229950002216 linifanib Drugs 0.000 claims description 4
- MPVGZUGXCQEXTM-UHFFFAOYSA-N linifanib Chemical compound CC1=CC=C(F)C(NC(=O)NC=2C=CC(=CC=2)C=2C=3C(N)=NNC=3C=CC=2)=C1 MPVGZUGXCQEXTM-UHFFFAOYSA-N 0.000 claims description 4
- 229950003968 motesanib Drugs 0.000 claims description 4
- RAHBGWKEPAQNFF-UHFFFAOYSA-N motesanib Chemical compound C=1C=C2C(C)(C)CNC2=CC=1NC(=O)C1=CC=CN=C1NCC1=CC=NC=C1 RAHBGWKEPAQNFF-UHFFFAOYSA-N 0.000 claims description 4
- 229950002212 mubritinib Drugs 0.000 claims description 4
- ZTFBIUXIQYRUNT-MDWZMJQESA-N mubritinib Chemical compound C1=CC(C(F)(F)F)=CC=C1\C=C\C1=NC(COC=2C=CC(CCCCN3N=NC=C3)=CC=2)=CO1 ZTFBIUXIQYRUNT-MDWZMJQESA-N 0.000 claims description 4
- 230000001575 pathological effect Effects 0.000 claims description 4
- 108091033319 polynucleotide Proteins 0.000 claims description 4
- 102000040430 polynucleotide Human genes 0.000 claims description 4
- 239000002157 polynucleotide Substances 0.000 claims description 4
- 229960003862 vemurafenib Drugs 0.000 claims description 4
- GPXBXXGIAQBQNI-UHFFFAOYSA-N vemurafenib Chemical compound CCCS(=O)(=O)NC1=CC=C(F)C(C(=O)C=2C3=CC(=CN=C3NC=2)C=2C=CC(Cl)=CC=2)=C1F GPXBXXGIAQBQNI-UHFFFAOYSA-N 0.000 claims description 4
- 206010059866 Drug resistance Diseases 0.000 claims description 3
- 108091027967 Small hairpin RNA Proteins 0.000 claims description 3
- 239000004055 small Interfering RNA Substances 0.000 claims description 3
- 108020004459 Small interfering RNA Proteins 0.000 claims description 2
- 238000002512 chemotherapy Methods 0.000 claims description 2
- 230000002452 interceptive effect Effects 0.000 claims description 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 9
- 201000010099 disease Diseases 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 238000001727 in vivo Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000001959 radiotherapy Methods 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161565226P | 2011-11-30 | 2011-11-30 | |
| US61/565,226 | 2011-11-30 | ||
| PCT/US2012/067403 WO2013082499A1 (en) | 2011-11-30 | 2012-11-30 | Targeting micrornas mir-409-5p, mir-379 and mir-154* to treat prostate cancer bone metastasis and drug resistant lung cancer |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2015504847A JP2015504847A (ja) | 2015-02-16 |
| JP2015504847A5 true JP2015504847A5 (enExample) | 2016-01-14 |
Family
ID=48536124
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014544946A Pending JP2015504847A (ja) | 2011-11-30 | 2012-11-30 | 前立腺癌骨転移および薬剤耐性肺癌を治療するためのマイクロｒｎａｍｉｒ−４０９−５ｐ、ｍｉｒ−３７９、およびｍｉｒ−１５４＊の標的化 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20140323551A1 (enExample) |
| EP (2) | EP2785355A4 (enExample) |
| JP (1) | JP2015504847A (enExample) |
| CN (1) | CN104080461A (enExample) |
| AU (1) | AU2012345666A1 (enExample) |
| WO (1) | WO2013082499A1 (enExample) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9745578B2 (en) | 2011-11-30 | 2017-08-29 | Cedars-Sinai Medical Center | Targeting microRNA miR-409-3P to treat prostate cancer |
| BR112015016282A2 (pt) * | 2013-01-07 | 2017-07-11 | Arog Pharmaceuticals Inc | crenolanibe para tratamento de distúrbios proliferativos de flt3 mutado |
| US10801071B2 (en) * | 2014-04-22 | 2020-10-13 | The Johns Hopkins University | TGF(β)-MIR200-MIG6 pathway and its use in the treatment of cancer as an indicator of resistance to EGFR inhibitors |
| US10493165B2 (en) | 2015-01-30 | 2019-12-03 | The Johns Hopkins University | Extracellular vesicles for agent delivery |
| EP3359553B1 (en) | 2015-10-06 | 2025-03-26 | University Of Virginia Patent Foundation | Compositions for treating diabetic retinopathy |
| EP3528803A4 (en) | 2016-10-21 | 2021-01-06 | Da Zen Theranostics, Inc | COMPOUNDS AND METHODS FOR Awareness Raising Of Cancer Cells To CISPLATIN |
| US11236337B2 (en) | 2016-11-01 | 2022-02-01 | The Research Foundation For The State University Of New York | 5-halouracil-modified microRNAs and their use in the treatment of cancer |
| US11584932B2 (en) | 2016-11-01 | 2023-02-21 | The Research Foundation For The State University Of New York | 5-halouracil-modified microRNAs and their use in the treatment of cancer |
| AU2018209164B2 (en) | 2017-01-17 | 2021-11-04 | Heparegenix Gmbh | Protein kinase inhibitors for promoting liver regeneration or reducing or preventing hepatocyte death |
| JP7164939B2 (ja) | 2017-08-25 | 2022-11-02 | 株式会社サムスン日本研究所 | 全固体型二次電池 |
| US10854877B2 (en) | 2017-08-25 | 2020-12-01 | Samsung Electronics Co., Ltd. | All-solid-state secondary battery |
| CN107488734B (zh) * | 2017-10-10 | 2019-11-05 | 广州医科大学附属第二医院 | miR-19a-3p在制备前列腺癌骨转移诊断试剂和治疗药物中的应用 |
| CN107630092B (zh) * | 2017-10-23 | 2020-03-31 | 广州医科大学附属第二医院 | miR-505-3p应用于前列腺癌骨转移的诊断、预后和治疗 |
| CN108148911B (zh) * | 2018-03-02 | 2019-11-05 | 广州医科大学附属第二医院 | miR-582在制备前列腺癌骨转移的诊断、预后试剂盒及药物中的应用 |
| KR102132222B1 (ko) * | 2018-11-27 | 2020-07-09 | 강원대학교산학협력단 | 항암제 내성 진단 마커로서의 miR-143-3p 및 miR-373-5p, 및 이의 이용 |
| CN110305863B (zh) * | 2019-06-10 | 2020-12-08 | 浙江大学 | 用于上调人DLK1-DIO3印记域非编码RNA表达的sgRNA、重组质粒和细胞株 |
| CN110819718B (zh) * | 2019-12-16 | 2023-05-26 | 广州医科大学附属第二医院 | miR-154-5p在前列腺癌骨转移的新应用 |
| EP4132942A4 (en) * | 2020-04-07 | 2024-05-01 | Advanced Cell Diagnostics, Inc. | IN SITU METHOD FOR DETECTING TARGET NUCLEIC ACIDS BY HYBRIDIZATION, AND ASSOCIATED KIT |
| WO2021262919A2 (en) | 2020-06-26 | 2021-12-30 | The Research Foundation For The State University Of New York | 5-halouracil-modified micrornas and their use in the treatment of cancer |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2322650A1 (en) * | 2004-05-14 | 2011-05-18 | Rosetta Genomics Ltd | MicroRNAs and uses thereof |
| EP2302053A1 (en) * | 2004-11-12 | 2011-03-30 | Asuragen, Inc. | Methods and compositions involving miRNA and miRNA inhibitor molecules |
| US20060265771A1 (en) * | 2005-05-17 | 2006-11-23 | Lewis David L | Monitoring microrna expression and function |
| US20070065844A1 (en) * | 2005-06-08 | 2007-03-22 | Massachusetts Institute Of Technology | Solution-based methods for RNA expression profiling |
| CA2617581A1 (en) * | 2005-08-01 | 2007-02-08 | The Ohio State University Research Foundation | Microrna-based methods for the diagnosis of breast cancer |
| CN101627121A (zh) * | 2006-12-08 | 2010-01-13 | 奥斯瑞根公司 | 作为治疗干预的靶标的miRNA调控基因和路径 |
| US20080311040A1 (en) * | 2007-03-06 | 2008-12-18 | Flagship Ventures | METHODS AND COMPOSITIONS FOR IMPROVED THERAPEUTIC EFFECTS WITH siRNA |
| MY156951A (en) * | 2007-10-04 | 2016-04-15 | Santaris Pharma As | Micromirs |
| CN104031984A (zh) * | 2008-02-28 | 2014-09-10 | 俄亥俄州立大学研究基金会 | 用于前列腺相关病症的诊断、预后和治疗的基于微rna的方法和组合物 |
| WO2010056737A2 (en) * | 2008-11-11 | 2010-05-20 | Mirna Therapeutics, Inc. | Methods and compositions involving mirnas in cancer stem cells |
| AU2010249421A1 (en) * | 2009-05-22 | 2011-12-08 | Asuragen, Inc. | miRNA biomarkers of prostate disease |
| CN102080085B (zh) * | 2009-12-01 | 2013-01-16 | 中国科学院上海药物研究所 | 人miR-193b反义核酸及其应用 |
| WO2011076142A1 (en) * | 2009-12-24 | 2011-06-30 | Fudan University | Compositions and methods for microrna expession profiling in plasma of colorectal cancer |
-
2012
- 2012-11-30 AU AU2012345666A patent/AU2012345666A1/en not_active Abandoned
- 2012-11-30 CN CN201280067969.XA patent/CN104080461A/zh active Pending
- 2012-11-30 WO PCT/US2012/067403 patent/WO2013082499A1/en not_active Ceased
- 2012-11-30 JP JP2014544946A patent/JP2015504847A/ja active Pending
- 2012-11-30 EP EP12854115.8A patent/EP2785355A4/en not_active Withdrawn
- 2012-11-30 US US14/360,489 patent/US20140323551A1/en not_active Abandoned
- 2012-11-30 EP EP16170595.9A patent/EP3106168A3/en not_active Withdrawn
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