Literature DB >> 12831361

Progress and challenges for cell encapsulation in brain tumour therapy.

Therese Visted1, Morten Lund-Johansen.   

Abstract

Cell encapsulation provides a method to circumvent the host immune system by encapsulating cells or tissues in immunoisolating, semipermeable membranes before implantation. The technology has been widely studied with an aim of developing bio-organs transplantable into patients without the need of immunosuppression, and in cancer therapy, the principle of cell encapsulation may be further exploited. Encapsulated recombinant cells represent factories or bioreactors for the production of therapeutic proteins. By implanting the bioreactors in the vicinity of the tumour, long-term local de novo delivery of the therapeutic proteins may be achieved. Malignant brain tumours such as glioblastoma multiforme (GBM) remain highly lethal neoplasms, refractory to current therapies. Researchers and medical professionals are working on developing translational therapies to combat these aggressive tumours. Numerous clinical trials on gene therapy for glioma patients have been conducted over the last decade, but the results have largely been disappointing. Cell encapsulation represents an alternative method for local delivery of therapeutic proteins with antineoplastic properties to glioma patients. The concept has not yet reached clinical trials, but encouraging results have been achieved in rats bearing gliomas when implanting endostatin-secreting encapsulated cells into the rat brain. This review primarily focuses on the recent progress that has been made with cell encapsulation technology. In addition, the challenges this field faces before clinical application in brain tumour patients is discussed.

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Year:  2003        PMID: 12831361     DOI: 10.1517/14712598.3.4.551

Source DB:  PubMed          Journal:  Expert Opin Biol Ther        ISSN: 1471-2598            Impact factor:   4.388


  5 in total

1.  NRG oncology RTOG 0625: a randomized phase II trial of bevacizumab with either irinotecan or dose-dense temozolomide in recurrent glioblastoma.

Authors:  Mark R Gilbert; Stephanie L Pugh; Ken Aldape; A Gregory Sorensen; Tom Mikkelsen; Marta Penas-Prado; Felix Bokstein; Young Kwok; R Jeffrey Lee; Minesh Mehta
Journal:  J Neurooncol       Date:  2016-10-21       Impact factor: 4.130

Review 2.  Clinical translation of stem cell therapy in traumatic brain injury: the potential of encapsulated mesenchymal cell biodelivery of glucagon-like peptide-1.

Authors:  Anna Heile; Thomas Brinker
Journal:  Dialogues Clin Neurosci       Date:  2011       Impact factor: 5.986

3.  Therapeutic concentrations of glucagon-like peptide-1 in cerebrospinal fluid following cell-based delivery into the cerebral ventricles of cats.

Authors:  Silke Glage; Petra M Klinge; Miles C Miller; Christine Wallrapp; Peter Geigle; Hans J Hedrich; Thomas Brinker
Journal:  Fluids Barriers CNS       Date:  2011-05-17

4.  Microtube Array Membrane (MTAM)-Based Encapsulated Cell Therapy for Cancer Treatment.

Authors:  Chee Ho Chew; Chih-Wei Lee; Wan-Ting Huang; Li-Wei Cheng; Amanda Chen; Tsai-Mu Cheng; Yen-Lin Liu; Chien-Chung Chen
Journal:  Membranes (Basel)       Date:  2020-04-26

5.  Type I collagen gene suppresses tumor growth and invasion of malignant human glioma cells.

Authors:  Kimi Honma; Teruo Miyata; Takahiro Ochiya
Journal:  Cancer Cell Int       Date:  2007-06-20       Impact factor: 5.722

  5 in total

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