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BioWorld - Saturday, June 27, 2026
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3D illustration of mitochondria.
Neurology/Psychiatric

Lucy Therapeutics validates new mitochondrial-based therapeutic approach for Parkinson's disease

Oct. 14, 2022
Lucy Therapeutics Inc. has announced promising preclinical data for multiple compounds in its lead program for Parkinson's disease, including two lead small-molecule agents, LucyTx-1209 and LucyTx-1212.
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Gastrointestinal

Researchers identify API5 as a γδ intraepithelial lymphocyte effector that enhances viability of Paneth cells

Oct. 14, 2022
Loss of Paneth cells and their antimicrobial granules has been linked to a compromised intestinal epithelial barrier, which is a hallmark of Crohn’s disease.
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Gastric cancer
Cancer

KL-6, a novel benzochalcone derivative with promising efficacy in gastric cancer models

Oct. 14, 2022
Chinese researchers have detailed the discovery of a novel benzochalcone derivative being developed for the treatment of gastric cancer.
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Close-up of elderly eye
Ocular

Exhaura presents data on EXH-001, an AAV9-hMMP-3 gene therapy for glaucoma treatment

Oct. 14, 2022
Glaucoma is an eye disease that damages the optic nerve, with the main cause being ocular hypertension due to high resistance to the outflow of aqueous humor.
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Human ossicle engrafted with human neuroblastoma cells.
Drug Design, Drug Delivery & Technologies

‘Mini-bones’ are metastasis model

Oct. 14, 2022
By Subhasree Nag
Investigators from the University of Copenhagen, Denmark have developed a cell line engineered to express bone morphogenetic protein 2 (BMP-2) and key extracellular matrix genes and critical factors that regulate and support human hematopoiesis. The findings were reported in the Oct. 12, 2022, issue of Science Translational Medicine. One of the clinical applications that the research team is interested in involves exploiting the MSOD-B hOss as a tumor model for bone colonization in the context of various cancers.
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Two mouse fibroblasts image captured using structured illumination microscopy.
Biomarkers

‘Quite dynamic’ senescent cells can participate in tissue repair

Oct. 14, 2022
By Mar de Miguel
Fibroblasts expressing the tumor suppressor p16INK4a (a marker of senescence) stimulated lung stem cells from young mice to repair damaged tissue, according to a study from the University of California, San Francisco (UCSF). The finding calls into question therapies that eliminate these senescent cells without considering their beneficial role in tissue homeostasis.
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Genetic/Congenital

Multi-ancestry biobanks identify multiple new targets

Oct. 13, 2022
By Anette Breindl
Scientists from the Global Biobank Meta-Analysis Initiative (GBMI) , founded in 2019, have published initial results in the Oct. 12, 2022 issue of Cell Genomics. In a series of papers, the investigators showed that the data collected by multiple biobanks could be harmonized and jointly analyzed, despite initial differences in recruitment strategies, sample collection, and definitions of diseases. Joint analysis identified new risk loci for more than a dozen common diseases, while another paper showed that such joint analysis could also be used to identify such loci for the rare disease idiopathic pulmonary fibrosis (IPF).
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Holiday notice

Oct. 13, 2022
In accordance with the publishing schedule, BioWorld Science was not published on Wednesday, Oct. 12, 2022.
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Illustration of cancer cells entering the bloodstream.
Biomarkers

BRMS1 single-nucleotide polymorphism increases metastasis risk in lung adenocarcinoma patients

Oct. 13, 2022
About 50% of patients with lung cancer present with metastatic disease; researchers have shown that breast cancer metastasis-suppressor 1 (BRMS1) suppresses metastases in non-small-cell lung cancer and other solid tumors due to its ability to function in a multiprotein histone deacetylase transcriptional corepressor complex or as an E3 ligase to control the degradation of p300 acetyltransferase.
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Muscular dystrophy
Neurology/Psychiatric

Metriopharm receives grant to support preclinical studies with MP-1032 for DMD

Oct. 13, 2022
Metriopharm AG has received a grant of €125,000 from charity Duchenne UK that will support development of the company's lead compound MP-1032 (luminol sodium salt) for the treatment of Duchenne muscular dystrophy (DMD).
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