GLYCANC · Matrix glycans as multifunctional pathogenesis factors and therapeutic targets in cancer
„Хоризонт 2020“ — Действия „Мария Склодовска-Кюри“
- Период
- 2015-07-01 → 2019-06-30
- Финансиране от ЕС
- 567 000 €
- Участници
- 13
- Схема
- MSCA-RISE
Линиите свързват координатора с партньорите.
Накратко на български
Специфични захари, наречени гликозаминагликани и протеогликани, влияят върху растежа и разпространението на туморите. Разбирането на техните функции помага за разработването на нови лекарства, които могат да преодолеят съпротивата на рака към съществуващата терапия.
Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.
Резултати накратко
Matrix glycans as multifunctional pathogenesis factors and therapeutic targets in cancer
Cancer is a leading cause of mortality within the aging European population and implies high costs for the general public. Eradication of cancer proves to be difficult, as disease mechanisms are complex. Not only molecular changes within the tumor, but also in the extracellular environment surrounding the tumor are important for the disease. This environment includes blood vessels and immune cells, which are hijacked and reprogrammed by the tumor to facilitate its growth. Recent research demonstrated that sugars called glycosaminoglycans (GAGs) and glycoproteins called proteoglycans (PGs) influence tumor growth and metastasis. As the role of these sugars in cancer has only been recently discovered, PG and GAG-based drugs will differ from existing drugs and may help to overcome resistance to therapy. We hypothesize that these drugs will stop multiple processes of cancer development and will therefore be superior to existing therapeutics. PGs and GAGs are currently under-investigated as their analysis is technically challenging. However, GLYCANC forms a team of specialists within the glycobiology field well-qualified to address this important research question. The understanding of the way these sugars work, and how this knowledge can be used for drug development was a major objective of GLYCANC. Other objectives were the development of new analytical technologies called spectroscopy and atomic force microscopy (AFM) to understand why they help tumor cells to grow and metastasis. Moreover, we wanted to understand new ways by which PGs and GAGs are regulated in a different way in cancer and normal cells by a process called epigenetics. With exchanges of university- and industry-based researchers between Europe, South America and Asia, GLYCANC has provided excellent interdisciplinary training for young scientists which became specialists in an upcoming and important research field. GLYCANC promoted the exchange of technologies and scientific ideas between industry and universities, leading to a more efficient research and a better qualification of all participants. As documented in 25 scientific publications so far, GLYCANC has substantially enhanced our understanding how proteoglycans regulate all relevant steps of tumor progression, has resulted in the development of new analytical techniques, and has resulted in the development of new glycoscience-based therapeutic approaches. As new proteoglycan targeting drugs have been successfully evaluated by the GLYCANC consortium in preclinical studies, the development of more efficient treatments can now proceed more rapidly, with considerable benefits for affected patients and society.
Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз
Цел на проекта
Cancer is a leading cause of mortality within the aging European population. Therapeutic targeting is hampered by the complexity of the disease, which includes not only molecular changes within the tumor cell itself, but also within its microenvironment. Tumor angiogenesis, tumor-stroma interactions, interactions with immune cells, with the extracellular matrix and cancer stem cell niches allow for malignant cell survival and promote metastasis, the leading cause for cancer-associated mortality. Proteoglycans (PGs) and glycosaminoglycans (GAGs) – structurally diverse carbohydrates of the extracellular matrix and cell surfaces - have emerged as novel biomarkers and molecular players both within tumor cells and their microenvironment, as they integrate signals from growth factors, chemokines and integrins, and cell-cell as well as matrix adhesion. Importantly, their expression is dysregulated in numerous tumor entities, and has been shown to modulate each of the hallmarks of cancer as defined by Hanahan and Weinberg (Cell 2011). We hypothesize that dysregulated function of PGs and GAGs simultaneously affects all molecular steps towards cancer metastasis as a general principle applicable to multiple tumor entities. Pharmacological modulation of their function thus emerges as an attractive multitargeted antitumoral approach which simultaneously acts at multiple levels of disease progression. Besides providing extensive knowledge transfer and training for researchers, the combined expertise of the GLYCANC consortium aims at performing a detailed structural analysis of PG and GAG glycans in disease using state-of-the art methodology, analysing their regulation via epigenetic mechanisms and microRNAs, and elucidating molecular mechanisms underlying aberrant PG and GAG function. GLYCANC will lead to a deeper understanding of glycan structures and glycan-dependent mechanisms promoting cancer progression, providing the basis for rational multitargeted anticancer approaches.
Оригинален текст от CORDIS (на английски).
Участници
- UNIVERSITAET MUENSTER · MuensterКоординаторГермания
- CAIRO UNIVERSITY · GizaЕгипет
- CONSEJO NACIONAL DE INVESTIGACIONES CIENTIFICAS Y TECNICAS (CONICET) · Buenos AiresАржентина
- EWHA WOMANS UNIVERSITY · SeoulЮжна Корея
- FIDIA FARMACEUTICI SPA · Abano TermeИталия
- NATIONAL CENTER FOR SCIENTIFIC RESEARCH ""DEMOKRITOS"""" · Agia ParaskeviГърция
- PANEPISTIMIO PATRON · RIO PATRASГърция
- SEMMELWEIS EGYETEM · BudapestУнгария
- SEREND-IP GMBH · MuensterГермания
- UNIVERSIDADE FEDERAL DO RIO DE JANEIRO · RIO DE JANEIROБразилия
- UNIVERSITA DEGLI STUDI DELL'INSUBRIA · VareseИталия
- UNIVERSITE DE REIMS CHAMPAGNE-ARDENNE · ReimsФранция
- UPPSALA UNIVERSITET · UppsalaШвеция
Връзки
- Виж в CORDIS
- DOI: 10.3030/645756
- https://campus.uni-muenster.de/glycanc/start/
- https://www.ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e5aa7fcb1c&appId=PPGMS
- https://www.ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e5aa7fcb1e&appId=PPGMS
- https://www.ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e5aa7fed5d&appId=PPGMS
- https://www.ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e5abd62186&appId=PPGMS
- https://www.ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e5acadc748&appId=PPGMS
- https://www.ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e5b1492cbe&appId=PPGMS
- https://www.ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e5b342cc98&appId=PPGMS
- https://www.ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e5b34372e4&appId=PPGMS
- https://www.ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e5b34378c6&appId=PPGMS
Данни: CORDIS, © Европейски съюз
