CN103961720A - Use of microRNA for preparing medicine lowering tolerance of neuroglioma to TRALL - Google Patents
Use of microRNA for preparing medicine lowering tolerance of neuroglioma to TRALL Download PDFInfo
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- CN103961720A CN103961720A CN201410165917.7A CN201410165917A CN103961720A CN 103961720 A CN103961720 A CN 103961720A CN 201410165917 A CN201410165917 A CN 201410165917A CN 103961720 A CN103961720 A CN 103961720A
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Abstract
The invention relates to use of a microRNA for preparing a medicine lowering the tolerance of neuroglioma to TRALL. The medicine comprises the microRNA of which the sequence is shown in the SEQ ID NO: 3; as the microRNA shown in the SEQ ID NO: 3 does not integrate with a DR5 gene 3'-UTR of a death receptor, the gene expression of the DR5 gene is improved and the tolerance of a tumor to the TRALL is lowered. The microRNA can adjust and control the gene expression of the DR5 gene, so as to adjust and control the tolerance of a tumor cell to the TRALL.
Description
The application is application number 201310089306.4, the applying date to be that on March 19th, 2013, denomination of invention are the divisional application of the application for a patent for invention of " medicine of a kind of modulate tumor to TRAIL toleration ".
Invention field
The present invention relates to biomedicine field, the medicine of the modulate tumor that especially contains microRNA to TRAIL toleration.
Background technology
Tumor necrosin relative death inducing ligand (TRAIL) is the newfound TNF newcomer of family in recent years, can induce in vitro kinds of tumor cells apoptosis, but normal tissue is insensitive.Show the safe and effective of it in the clinical I of U.S. phase experimental data, carried out at present II/III phase clinical research.TRAIL is mainly by bringing into play the function of cell death inducing with the receptors bind of cell surface, death receptor DR4 and DR5 are 2 specific receptors of TRAIL, because these two receptors exist only in tumor, so TRAIL has no side effect to normal cell.Although TRAIL provides new approach for oncotherapy, but find in clinical and laboratory research, nearly 50% tumor cell has certain toleration to TRAIL, and while going to process tumor cell with TRAIL, tumor cell does not have obvious apoptosis phenomenon to occur.
MicroRNA (miRNA) is that length is the little RNA of non-coding of 20～24 nucleotide, can be by the expression of inhibition target gene specific with the combination of target spot.Nearly ten years, researcher finds that microRNA is bringing into play extremely important function in the physiological process such as propagation, differentiation and the apoptosis of fetal development and cell.Up to the present, there is the toleration of several microRNA energy modulate tumors to TRAIL, for example, microRNA-221/222 can be expressed and be weakened therapeutic effect (the Garofalo M of TRAIL to nonsmall-cell lung cancer by downward PTEN and TIMP3, Di Leva G, Romano G, Nuovo G, Suh SS, Ngankeu A, Taccioli C, Pichiorri F, Alder H, Secchiero P, Gasparini P, GonelliA, Costinean S, Acunzo M, Condorelli G, Croce CM.miR-221 & 222regulate TRAIL resistanceand enhance tumorigenicity through PTEN and TIMP3downregulation.Cancer Cell2009, 16:498-509), and it is contrary, microRNA-130 and microRNA-212 can improve sensitivity (the Incoronato M of tumor cell to TRAIL by target PED, Garofalo M, Urso L, Romano G, Quintavalle C, Zanca C, Iaboni M, Nuovo G, Croce CM, Condorelli G.miR-212increases tumor necrosis factor-relatedapoptosis-inducing ligand sensitivity in non-small cell lung cancer by targeting the antiapoptoticprotein PED.Cancer Res2010, 70:3638-3646.Acunzo M, Visone R, Romano G, Veronese A, Lovat F, Palmieri D, Bottoni A, Garofalo M, Gasparini P, Condorelli G, Chiariello M, Croce CM.miR-130a targets METand induces TRAIL-sensitivity in NSCLC by downregulating miR-221and222.Oncogene2012, 31:634-642).Recently, microRNA-25 is in the news and can improves toleration (the Razumilava N of cholangiocarcinoma cell to TRAIL by the expression of regulation and control DR4, Bronk SF, Smoot RL, Fingas CD, Werneburg NW, Roberts LR, Mott JL.miR-25targets TNF-related apoptosis inducing ligand (TRAIL) death receptor-4and promotesapoptosis resistance in cholangiocarcinoma.Hepatology2012; 55:465-475).
Summary of the invention
Therefore, for tumor cell, TRAIL is there is the problem of toleration, the invention provides the medicine of the modulate tumor that contains microRNA to TRAIL toleration.
To achieve these goals, the present invention adopts following technical scheme.
The medicine of modulate tumor to TRAIL toleration, is characterized in that, it is microRNA and variant thereof shown in SEQ ID NO:1-4 that described medicine contains sequence.
Preferably, microRNA and variant thereof shown in SEQ ID NO:1-2 are combined with death receptor DR5 gene 3 '-UTR, suppress the expression of DR5 gene, improve the toleration of tumor to TRAIL.
Preferably, microRNA and variant thereof shown in SEQ ID NO:3-4 are not combined with death receptor DR5 gene 3 '-UTR, improve the expression of DR5 gene, reduce the toleration of tumor to TRAIL.
Preferably, the microRNA shown in SEQ ID NO:1 is microRNA-133a; MicroRNA shown in SEQ ID NO:2 is microRNA-133b.
Preferably, the antisense sequences that the microRNA shown in SEQ ID NO:3 is microRNA-133a; The antisense sequences that microRNA shown in SEQ ID NO:4 is microRNA-133b.
Preferably, described microRNA obtains by chemosynthesis or from organism sample.
Further preferably, described organism sample is tissue or cell.
Preferably, described microRNA is a kind of diagnostic markers or treatment target of TRAIL treatment.
Preferably, described tumor comprises all solid tumors and leukemia.
Further preferably, described tumor is glioma.
The medicine of modulate tumor of the present invention to TRAIL toleration, contained microRNA and antisense sequences thereof, by the regulation and control to DR5 gene expression, reach the object of modulate tumor cell to TRAIL toleration.Thereby described microRNA can improve the toleration of TRAIL in neuroglial cytoma by reducing the expression of DR5, and its antisense sequences has significantly improved the expression of DR5 and promoted the apoptosis that TRAIL induces.So microRNA-133a/b is likely as diagnostic markers or the molecular target of TRAIL oncotherapy.
Brief description of the drawings
Fig. 1 is the toleration figures of 5 kinds of neuroglial cytomas to TRAIL.Wherein, in Fig. 1, A is the propagation result that mtt assay is measured 5 kinds of neuroglial cytomas; In Fig. 1, B is the apoptosis result of 5 kinds of neuroglial cytomas of PI Determination Staining.
Fig. 2 is the expression of results figure of microRNA in the neuroglial tumor of different TRAIL tolerance types.
Fig. 3 is the schematic diagram that bioinformatics software prediction microRNA is combined with DR5.
Fig. 4 is the data result figure that extracorporeal biology functional experiment checking microRNA is combined with DR5.
Fig. 5 be the TRAIL of microRNA-133a on neuroglial cytoma toleration affect result figure.
In above-mentioned figure, U87, M059K, M059J, A172 and T98G are neuroglial cytoma strain in 5, purchased from US mode culture collection warehousing (American type culture collection, ATCC); MiR-133a represents microRNA-133a, and miR-133b represents microRNA-133b, and anti-133a represents the antisense sequences of microRNA-133a; Mock represents blank, and NC represents negative control.
Detailed description of the invention
Below in conjunction with specific embodiment, such scheme is described further.Should be understood that these embodiment do not limit the scope of the invention for the present invention is described.The implementation condition adopting in embodiment can be done further adjustment as the case may be, and not marked implementation condition is generally the condition in normal experiment.
" microRNA " in the present invention can be chemosynthesis, can be also to extract cell from there is this gene order, tissue.Described tissue can select neoplastic lesion tissue, and paraffin mass, the paraffin section made with these tissues.
" sample " in the present invention refers to potential all in vitro samples that may contain sequence shown in SEQ ID NO:1-4, preferably from the sample of human body.More preferably from the sample of tumor tissues.Certainly the purification of samples of the total RNA of blood extracting also can be served as sample of the present invention.
" microRNA-133a " in the present invention refers to and comprises the sequence shown in SEQ ID NO:1 or the microRNA of its homologous sequence.The microR-133a in known various sources in this area, such as people, chimpanzee, Mus etc., these homologous sequences are all included in term of the present invention " microRNA-133a ".In the present invention, microRNA-133a variant comprises process in above-mentioned naturally occurring microRNA-133a sequence and replaces, lacks or add one or several nucleotide, or process biochemical modification, and still has the derivative RNA of biologic activity.The meaning of the antisense sequences of MicroRNA-133b, microRNA-133a and the antisense sequences of microRNA-133b and their variant and scope are with reference to above-mentioned explanation.
" oncotherapy " in the present invention refers to various solid tumors and leukemia, preferably glioma.
" medicine " of " medicine of modulate tumor to TRAIL toleration " in the present invention can also comprise other active component or the auxiliary element for the treatment of or prophylaxis of tumours.
The toleration of embodiment mono-, neuroglial cytoma TRAIL
Taking 5 kinds of common neuroglial cytomas as model, with the TRAIL (50ng/ml of variable concentrations; 100ng/ml) process respectively 5 kinds of neuroglial cytomas toleration to TRAIL that adopted cell proliferation (mtt assay) and PI Determination Staining.Statistical analysis discovery, taking U87 cell as standard, M059K and M059J belong to TRAIL tolerance type cell strain, and A172 and T98G belong to TRAIL responsive type cell strain.The results are shown in Figure 1.
Embodiment bis-, the microRNA-133a/b expression in the neuroglial cytoma of different TRAIL tolerance types
Adopt Real-Time Fluorescent Quantitative PCR Technique to measure microRNA-133a and the expression of microRNA-133b in the neuroglial cytoma of different TRAIL tolerance types.Statistical analysis discovery, microRNA-133a and microRNA-133b express and are raised in TRAIL tolerance type cell strain; And in the cell strain of TRAIL responsive type, express suppressed.The results are shown in Figure 2.
Embodiment tri-, Bioinformatics Prediction microRNA-133a may be combined with DR5 gene 3 '-UTR
Adopt bioinformatics software TargetScan prediction to find, hsa-microRNA-133a may be combined with DR5 gene 3 '-UTR, the results are shown in Figure shown in 3.
Embodiment tetra-, extracorporeal biology experimental results show that microRNA-133a suppresses the expression of DR5
MicroRNA-133a is transfected into respectively to U87, M059J and A172 cell are interior after 72 hours, collecting cell, extract respectively RNA and albumen and carry out the expression of Q-PCR and Western blotting detection DR5, result shows no matter at mRNA level or protein level, microRNA-133a significantly lowers the expression of DR5, and the antisense sequences of microRNA-133a (anti-microRNA-133a) but raises its expression.Therefore, above-mentioned extracorporeal biology functional experiment confirmation, microRNA-133a can be combined with DR5 gene 3 '-UTR, thereby suppresses the expression of DR5, the results are shown in Figure 4.
The impact of embodiment five, the microRNA-133a TRAIL toleration on neuroglial cytoma
Adopt cell proliferation (mtt assay) and PI Determination Staining the impact of the TRAIL toleration of microRNA-133a on neuroglial cytoma.Statistical analysis, microRNA-133a has increased the toleration of the TRAIL of neuroglial cytoma, and its antisense sequences has reduced the toleration of the TRAIL of neuroglial cytoma, has promoted the apoptosis of TRAIL induction.The results are shown in Figure 5.
Above-mentioned example is only explanation technical conceive of the present invention and feature, and its object is to allow person skilled in the art can understand content of the present invention and implement according to this, can not limit the scope of the invention with this.All equivalent transformations that spirit is done according to the present invention or modification, within all should being encompassed in protection scope of the present invention.
Claims (6)
- MicroRNA shown in 1.SEQ ID NO:3 is for the preparation of the purposes that reduces the medicine of glioma to TRAIL toleration.
- 2. purposes according to claim 1, is characterized in that, microRNA shown in SEQ ID NO:3 is not combined with death receptor DR5 gene 3 '-UTR, improves the expression of DR5 gene, reduces the toleration of tumor to TRAIL.
- 3. purposes according to claim 1, is characterized in that, the antisense sequences that shown in SEQ ID NO:3, microRNA is microRNA-133a.
- 4. purposes according to claim 1, is characterized in that, described microRNA obtains by chemosynthesis or from organism sample.
- 5. purposes according to claim 4, is characterized in that, described organism sample is tissue or cell.
- 6. purposes according to claim 1, is characterized in that, described microRNA is a kind of diagnostic markers or treatment target of TRAIL treatment.
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| Application Number | Priority Date | Filing Date | Title |
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| CN201410165917.7A CN103961720B (en) | 2013-03-19 | 2013-03-19 | MicroRNA is for the preparation of reducing glioma to the purposes of the medicine of TRAIL toleration |
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| CN201410165917.7A CN103961720B (en) | 2013-03-19 | 2013-03-19 | MicroRNA is for the preparation of reducing glioma to the purposes of the medicine of TRAIL toleration |
| CN201310089306.4A CN103157117B (en) | 2013-03-19 | 2013-03-19 | Medicine for regulating and controlling TRAIL (Tnf (Tumor necrosis factor) Related Apoptosis Inducing Ligand) tolerance of tumour |
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Citations (4)
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| WO2010041140A2 (en) * | 2008-10-10 | 2010-04-15 | National University Of Ireland | Treatment of proliferative disorders with a death receptor agonist |
| CN102080086A (en) * | 2009-12-01 | 2011-06-01 | 中国科学院上海药物研究所 | Human miR-133a antisense nucleic acid and application thereof |
| CN102573856A (en) * | 2009-09-10 | 2012-07-11 | 弗莱明·韦林 | Method for the preparation of micro-RNAand its therapeutic application |
| CN102803511A (en) * | 2009-11-23 | 2012-11-28 | 俄亥俄州立大学 | Materials and methods useful for affecting tumor cell growth, migration and invasion |
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Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010041140A2 (en) * | 2008-10-10 | 2010-04-15 | National University Of Ireland | Treatment of proliferative disorders with a death receptor agonist |
| CN102573856A (en) * | 2009-09-10 | 2012-07-11 | 弗莱明·韦林 | Method for the preparation of micro-RNAand its therapeutic application |
| CN102803511A (en) * | 2009-11-23 | 2012-11-28 | 俄亥俄州立大学 | Materials and methods useful for affecting tumor cell growth, migration and invasion |
| CN102080086A (en) * | 2009-12-01 | 2011-06-01 | 中国科学院上海药物研究所 | Human miR-133a antisense nucleic acid and application thereof |
Non-Patent Citations (4)
| Title |
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| EUN MI JUNG等: "Curcumin sensitizes tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-induced apoptosis through reactive oxygen species-mediated upregulation of death receptor 5 (DR5)", 《CARCINOGENESIS》, 29 June 2005 (2005-06-29), pages 1905 - 1913 * |
| JUAN P. PATRON等: "MiR-133b Targets Antiapoptotic Genes and Enhances Death Receptor-Induced Apoptosis", 《PLOSONE》, 20 April 2012 (2012-04-20) * |
| M GAROFALO等: "MicroRNA signatures of TRAIL resistance in human non-small cell lung cancer", 《ONCOGENE》, vol. 27, 4 February 2008 (2008-02-04), pages 3845 - 3855, XP008157324, DOI: doi:10.1038/onc.2008.6 * |
| NATALIYA RAZUMILAVA等: "miR-25 targets TNF-related apoptosis inducing ligand (TRAIL) death receptor-4 and promotes apoptosis resistance in cholangiocarcinoma", 《HEPATOLOGY》, 31 December 2012 (2012-12-31), pages 465 - 475 * |
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| CN103961720B (en) | 2016-03-02 |
| CN103157117A (en) | 2013-06-19 |
| CN103157117B (en) | 2014-07-02 |
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