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- Publisher Website: 10.1158/0008-5472.SABCS11-P4-08-05
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Conference Paper: Diagnostic Significance of Exosomal miRNAs in the Plasma of Breast Cancer Patients
Title | Diagnostic Significance of Exosomal miRNAs in the Plasma of Breast Cancer Patients |
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Authors | |
Publisher | American Association for Cancer Research. The Journal's web site is located at http://cancerres.aacrjournals.org/ |
Citation | The 34th Annual CTRC-AACR San Antonio Breast Cancer Symposium (SABCS 2011), San Antonio, TX., 6-10 December 2011. In Cancer Research, 2011, v. 71 n. 24 suppl., abstract no. P4-08-05 How to Cite? |
Abstract | Background and Aims: Emerging evidence that microRNAs (miRNAs) play an important role in cancer development has opened up new opportunities for cancer diagnosis. Recent studies demonstrated that released exosomes which contain a subset of both cellular mRNA and miRNA could be a useful source of biomarkers for cancer detection. Here, we aim to develop a novel biomarker for breast cancer diagnosis using exosomal miRNAs in plasma. Methods: We have developed a rapid and novel isolation protocol to enrich tumor-associated exosomes from plasma samples by capturing tumor specific surface markers containing exosomes. After enrichment, we performed miRNA profiling on four sample sets; (1) Ep-CAM marker enriched plasma exosomes of breast cancer patients; (2) breast tumors of the same patients; (3) adjacent non-cancerous tissues of the same patients; (4) Ep-CAM marker enriched plasma exosomes of normal control subjects. Profiling is performed using PCR-based array with human microRNA panels that contain more than 700 miRNAs.
Results: Our profiling data showed that 15 miRNAs are concordantly up-regulated and 13 miRNAs are concordantly down-regulated in both plasma exosomes and corresponding tumors. These account for 25% (up-regulation) and 15% (down-regulation) of all miRNAs detectable in plasma exosomes. Our findings demonstrate that miRNA profile in EpCAM-enriched plasma exosomes from breast cancer patients exhibit certain similar pattern to that in the corresponding tumors. Based on our profiling results, plasma signatures that differentiated breast cancer from control are generated and some of the well-known breast cancer related miRNAs such as miR-10b, miR-21, miR-155 and miR-145 are included in our panel list. The putative miRNA biomarkers are validated on plasma samples from an independent cohort from more than 100 cancer patients. Further validation of the selected markers is likely to offer an accurate, noninvasive and specific diagnostic assay for breast cancer.
Conclusions: These results suggest that exosomal miRNAs in plasma may be a novel biomarker for breast cancer diagnosis. |
Description | Poster Session Abstracts |
Persistent Identifier | http://hdl.handle.net/10722/196734 |
ISSN | 2023 Impact Factor: 12.5 2023 SCImago Journal Rankings: 3.468 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Kwong, A | - |
dc.contributor.author | Ng, EKO | - |
dc.contributor.author | Leung, CPH | - |
dc.contributor.author | Chan, V | - |
dc.contributor.author | Li, R | - |
dc.contributor.author | Wong, CLP | - |
dc.contributor.author | Ma, ESK | - |
dc.date.accessioned | 2014-04-25T04:47:52Z | - |
dc.date.available | 2014-04-25T04:47:52Z | - |
dc.identifier.citation | The 34th Annual CTRC-AACR San Antonio Breast Cancer Symposium (SABCS 2011), San Antonio, TX., 6-10 December 2011. In Cancer Research, 2011, v. 71 n. 24 suppl., abstract no. P4-08-05 | - |
dc.identifier.issn | 0008-5472 | - |
dc.identifier.uri | http://hdl.handle.net/10722/196734 | - |
dc.description | Poster Session Abstracts | - |
dc.description.abstract | Background and Aims: Emerging evidence that microRNAs (miRNAs) play an important role in cancer development has opened up new opportunities for cancer diagnosis. Recent studies demonstrated that released exosomes which contain a subset of both cellular mRNA and miRNA could be a useful source of biomarkers for cancer detection. Here, we aim to develop a novel biomarker for breast cancer diagnosis using exosomal miRNAs in plasma. Methods: We have developed a rapid and novel isolation protocol to enrich tumor-associated exosomes from plasma samples by capturing tumor specific surface markers containing exosomes. After enrichment, we performed miRNA profiling on four sample sets; (1) Ep-CAM marker enriched plasma exosomes of breast cancer patients; (2) breast tumors of the same patients; (3) adjacent non-cancerous tissues of the same patients; (4) Ep-CAM marker enriched plasma exosomes of normal control subjects. Profiling is performed using PCR-based array with human microRNA panels that contain more than 700 miRNAs. Results: Our profiling data showed that 15 miRNAs are concordantly up-regulated and 13 miRNAs are concordantly down-regulated in both plasma exosomes and corresponding tumors. These account for 25% (up-regulation) and 15% (down-regulation) of all miRNAs detectable in plasma exosomes. Our findings demonstrate that miRNA profile in EpCAM-enriched plasma exosomes from breast cancer patients exhibit certain similar pattern to that in the corresponding tumors. Based on our profiling results, plasma signatures that differentiated breast cancer from control are generated and some of the well-known breast cancer related miRNAs such as miR-10b, miR-21, miR-155 and miR-145 are included in our panel list. The putative miRNA biomarkers are validated on plasma samples from an independent cohort from more than 100 cancer patients. Further validation of the selected markers is likely to offer an accurate, noninvasive and specific diagnostic assay for breast cancer. Conclusions: These results suggest that exosomal miRNAs in plasma may be a novel biomarker for breast cancer diagnosis. | - |
dc.language | eng | - |
dc.publisher | American Association for Cancer Research. The Journal's web site is located at http://cancerres.aacrjournals.org/ | - |
dc.relation.ispartof | Cancer Research | - |
dc.title | Diagnostic Significance of Exosomal miRNAs in the Plasma of Breast Cancer Patients | en_US |
dc.type | Conference_Paper | en_US |
dc.identifier.email | Kwong, A: avakwong@hkucc.hku.hk | - |
dc.identifier.email | Ng, EKO: ngko@hku.hk | - |
dc.identifier.email | Chan, V: vnychana@hkucc.hku.hk | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1158/0008-5472.SABCS11-P4-08-05 | - |
dc.identifier.volume | 71 | - |
dc.identifier.issue | 24 suppl. | - |
dc.identifier.isi | WOS:000209699801277 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 0008-5472 | - |