H2020Индивидуална стипендия2019–2021

BrEXo-Apt · Non-invasive and accurate diagnosis and treatment of breast cancer.

„Хоризонт 2020“ — Действия „Мария Склодовска-Кюри“

Период
2019-04-01 → 2021-03-31
Финансиране от ЕС
187 572 €
Участници
1
Схема
MSCA-IF

Линиите свързват координатора с партньорите.

Накратко на български

Екзозомите (малки везикули от туморни клетки) и специални молекули, наречени аптамери, се изследват за по-точно откриване на рак на гърдата. Ранната диагностика чрез тези биомаркери помага за откриване на туморите в етап, в който са най-лесно лечими.

Този кратък обзор е генериран от изкуствен интелект

Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.

Резултати накратко

Non-invasive and accurate diagnosis and treatment of breast cancer.

“BrEXo-Apt” is about non-invasive and accurate diagnosis and treatment of breast cancer (BC). Early screening methods for BC are mainly based on instrumental tests, that may cause in many cases a failure to reach particular categories of patients. This failure could be overcome with the availability of specific and predictive circulating biomarkers allowing non-invasive earliest tumour detection on a larger scale of patients. Recent evidences indicate that the release of a great numbers of exosomes by tumour cells play a key role in tumour progression, drug resistance, immune surveillance escape, angiogenesis, tumour invasion and metastasis. For this reason, cancer-derived exosomes are emerging as very interesting targets for cancer therapy and diagnosis. BC is the most common tumour type and one of the leading causes of cancer mortality in women with more than 450,000 women die annually. The disease stage at diagnosis greatly influences patient survival. Although traditional diagnostic methods, such as mammography, are effective, they are limited by the minimum tumour size required for detection. Therefore, the research of circulating biomarkers is a fundamental challenge that can allow to find out tumours early, when they are non-invasive and most treatable, consequently improving disease outcome and health costs. Aptamers are high affinity ligands of disease-associated proteins and possess many advantages for diagnostic and therapeutic applications including low toxicity, cost-effectiveness, easy synthesis and modification, associated with no immunogenicity. The specific targeting ability of aptamers has ensured their efficient use for biomarker discovery, detection and profiling. In recent years, extracellular endosome-derived vesicles called exosomes are attracting growing interest as promising cancer biomarkers. Exosomes are vesicles of 50–150 nm diameter secreted by cells into circulation and containing nucleic acids and proteins. It has been demonstrated that tumour cells, including BC cells, release excessive amounts of cell specific exosomes that, being stable and easily accessible from body fluids, may be used for cancer specific detection. In addition, cancer exosome involvement in tumour progression and dissemination, drug resistance and immune surveillance. “BrEXo-Apt” took advantage of a novel class of nucleic acid-based molecules named aptamers to specifically identified and inhibit BC exosome and permit early BC detection and early therapeutic treatment. “BrEXo-Apt” used BC aptamers that specifically recognize BC-released exosomes to an early BC diagnosis and treatment. The rationale of our study was that in BC field, non-invasive modality of tumours early diagnosis and target therapy are urgently needed. Aptamers show proprieties that can be easily be applied to this issue. The objective was to develop an innovative, non-invasive approach for early BC detection and its treatment. Towards this question Dr Quintavalle proposed to develop an aptamer-based sandwich assay able to recognize BC-derived exosomes in blood and an aptamer-based affinity plasmapheresis system able to specifically remove BC-derived exosomes.

Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз

Цел на проекта

Increasing evidences indicate that the release of a great numbers of exosomes by tumour cells play a key role in tumour progression, drug resistance, immune surveillance escape, angiogenesis, tumour invasion and metastasis. For this reason, cancer-derived exosomes are emerging as very interesting targets for cancer therapy and diagnosis. In particular, extracellular exosomes may have great potential as early diagnostic and prognostic biomarkers for many types of cancer, including breast cancer. Early screening methods for breast cancer are mainly based on instrumental tests, that may cause in many cases a failure to reach particular categories of patients. This failure could be overcome with the availability of specific and predictive circulating biomarkers allowing non-invasive earliest tumour detection on a larger scale of patients. Indeed, progresses in developing nucleic acids-based therapeutic compounds, including antisense DNAs, aptamers, short interfering/microRNAs, and short activator RNAs, have attracted great interest as emerging platforms for precise cancer treatment. Dr Quintavalle has identified aptamers that specifically recognize BC-released exosomes and are able to discriminate between breast cancer derived exosome and glioma or lung cancer derived exosomes. Preliminary data indicates also that these aptamers are able to block the internalization of MDA231 derived exosome on MDA231 cells. To develop a new diagnostic and therapeutic strategy, Dr Quintavalle will aim to exploit the identified aptamers to design an innovative aptamer-based sandwich assay for their specific detection in patient blood samples. Moreover, since the inhibition of cancer exosome uptake by surrounding healthy tissues and organs would represent an effective strategy to interfere with tumour spreading and development, Dr. Quintavalle will aim to generate an affinity plasmapheresis system by using BC specific aptamers for specifically remove BC-derived exosome from patient blood.

Оригинален текст от CORDIS (на английски).

Участници

Връзки

Данни: CORDIS, © Европейски съюз