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- Publisher Website: 10.1007/978-1-62703-456-2_14
- Scopus: eid_2-s2.0-84929860833
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Book Chapter: Chemoresistance in glioma
Title | Chemoresistance in glioma |
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Authors | |
Keywords | Blood-brain barrier Cancer stem cells Chemoresistance Chemotherapeutic agent DNA repair Glioma Hypoxia microRNA Temozolomide |
Issue Date | 2013 |
Publisher | Humana Press |
Citation | Chemoresistance in glioma. In Lee, NP ... (et al) (Eds.), New advances on disease biomarkers and molecular targets in biomedicine, p. 243-270. New York: Humana Press, 2013 How to Cite? |
Abstract | Glioma remains one of the most aggressive and lethal form of cancer. Despite the best available treatment options including surgical resection, radiotherapy, and chemotherapy, prognosis is poor with a median overall survival of just over 1 year. Most patients would die of tumour recurrences because of their tumours’ intrinsic or acquired resistance against chemotherapy. Researchers have strived to better understand the molecular mechanisms of chemoresistance in glioma by using different experimental models, and to direct targeted therapeutics in an attempt to overcome treatment resistance. Currently, different pathways that can confer drug resistance have been identified including DNA damage repair, drug efflux, hypoxia, cancer stem cells, and microRNAs (miRNAs). This chapter will discuss how modulation of these signalling pathways may potentially lead to the development of novel approaches for the treatment of this condition. |
Persistent Identifier | http://hdl.handle.net/10722/187476 |
ISBN |
DC Field | Value | Language |
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dc.contributor.author | Sun, S | en_US |
dc.contributor.author | Lee, D | en_US |
dc.contributor.author | Leung, GKK | en_US |
dc.date.accessioned | 2013-08-20T12:50:33Z | - |
dc.date.available | 2013-08-20T12:50:33Z | - |
dc.date.issued | 2013 | en_US |
dc.identifier.citation | Chemoresistance in glioma. In Lee, NP ... (et al) (Eds.), New advances on disease biomarkers and molecular targets in biomedicine, p. 243-270. New York: Humana Press, 2013 | en_US |
dc.identifier.isbn | 9781627034555 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/187476 | - |
dc.description.abstract | Glioma remains one of the most aggressive and lethal form of cancer. Despite the best available treatment options including surgical resection, radiotherapy, and chemotherapy, prognosis is poor with a median overall survival of just over 1 year. Most patients would die of tumour recurrences because of their tumours’ intrinsic or acquired resistance against chemotherapy. Researchers have strived to better understand the molecular mechanisms of chemoresistance in glioma by using different experimental models, and to direct targeted therapeutics in an attempt to overcome treatment resistance. Currently, different pathways that can confer drug resistance have been identified including DNA damage repair, drug efflux, hypoxia, cancer stem cells, and microRNAs (miRNAs). This chapter will discuss how modulation of these signalling pathways may potentially lead to the development of novel approaches for the treatment of this condition. | - |
dc.language | eng | en_US |
dc.publisher | Humana Press | en_US |
dc.relation.ispartof | New advances on disease biomarkers and molecular targets in biomedicine | en_US |
dc.subject | Blood-brain barrier | - |
dc.subject | Cancer stem cells | - |
dc.subject | Chemoresistance | - |
dc.subject | Chemotherapeutic agent | - |
dc.subject | DNA repair | - |
dc.subject | Glioma | - |
dc.subject | Hypoxia | - |
dc.subject | microRNA | - |
dc.subject | Temozolomide | - |
dc.title | Chemoresistance in glioma | en_US |
dc.type | Book_Chapter | en_US |
dc.identifier.email | Sun, S: ssun@hku.hk | en_US |
dc.identifier.email | Lee, D: leederek@hku.hk | en_US |
dc.identifier.email | Leung, GKK: gilberto@hkucc.hku.hk | en_US |
dc.identifier.authority | Leung, GKK=rp00522 | en_US |
dc.identifier.doi | 10.1007/978-1-62703-456-2_14 | - |
dc.identifier.scopus | eid_2-s2.0-84929860833 | - |
dc.identifier.hkuros | 218592 | en_US |
dc.identifier.spage | 243 | en_US |
dc.identifier.epage | 270 | en_US |
dc.publisher.place | New York | en_US |