Joana Borlido

ORCID: 0000-0003-2622-0901
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About
Contact & Profiles
Research Areas
  • Nuclear Structure and Function
  • RNA Research and Splicing
  • RNA modifications and cancer
  • Cellular transport and secretion
  • Genetic Associations and Epidemiology
  • Microtubule and mitosis dynamics
  • Bioinformatics and Genomic Networks
  • Mitochondrial Function and Pathology
  • RNA regulation and disease
  • Monoclonal and Polyclonal Antibodies Research
  • Trace Elements in Health
  • Retinal Development and Disorders
  • Metabolism, Diabetes, and Cancer
  • Muscle Physiology and Disorders
  • Cancer, Hypoxia, and Metabolism
  • CAR-T cell therapy research
  • Ubiquitin and proteasome pathways
  • T-cell and B-cell Immunology
  • Biotin and Related Studies
  • Adipose Tissue and Metabolism
  • Peptidase Inhibition and Analysis
  • Nutrition, Genetics, and Disease

Pfizer (United States)
2023-2024

Discovery Institute
2017-2023

Sanford Burnham Prebys Medical Discovery Institute
2017-2023

University of Cambridge
2014

Cardiovascular Institute Hospital
2013

Institute of Molecular Biology and Biophysics
2013

University of California, San Francisco
2013

Cancer Research UK
2008-2009

Circulating proteins can reveal key pathways to cancer and identify therapeutic targets for prevention. We investigate 2,074 circulating risk of nine common cancers (bladder, breast, endometrium, head neck, lung, ovary, pancreas, kidney, malignant non-melanoma) using cis protein Mendelian randomisation colocalization. conduct additional analyses adverse side-effects altering map drug targets. Here we find 40 associated with cancers, such as PLAUR breast [odds ratio per standard deviation...

10.1038/s41467-024-46834-3 article EN cc-by Nature Communications 2024-04-29

Article16 May 2014Open Access Source Data Nuclear ARRB1 induces pseudohypoxia and cellular metabolism reprogramming in prostate cancer Vincent Zecchini Corresponding Author Department of CRUK, CRUK Cambridge Institute, University Cambridge, UK Search for more papers by this author Basetti Madhu Roslin Russell Nelma Pértega-Gomes Life Health Sciences Research School Sciences, Minho, Braga, Portugal Anne Warren Pathology, Edoardo Gaude Medical Council Cancer Cell Unit, Hutchison/MRC Centre,...

10.15252/embj.201386874 article EN cc-by The EMBO Journal 2014-05-16

Background Clathrin is a multimeric protein involved in vesicle coat assembly. Recently clathrin distribution was reported to change during the cell cycle and found associate with mitotic spindle. Here we test whether recruitment of spindle indicative critical functional contribution mitosis. Methodology/Principal Findings Previously chicken pre-B lymphoma line (DKO-R) developed which endogenous heavy chain alleles were replaced human under control tetracycline-regulatable promoter....

10.1371/journal.pone.0003115 article EN cc-by PLoS ONE 2008-09-02

Abstract Background Understanding the role of circulating proteins in cancer risk can reveal key biological pathways and identify novel therapeutic targets for prevention. Methods We investigated associations 2,094 with nine common cancers (bladder, breast, endometrium, head neck, lung, ovary, pancreas, kidney, malignant non-melanoma) using cis pQTL Mendelian randomisation (MR) colocalization. Findings support from both MR, after correction multiple-testing, colocalization were replicated an...

10.1101/2023.05.05.23289547 preprint EN cc-by-nd medRxiv (Cold Spring Harbor Laboratory) 2023-05-14

Abstract PF-07062119 (GUCY2C x CD3), a bispecific T cell engager (TCE) targeting Guanylyl Cyclase C (GUCY2C), GI tumor associated antigen, is currently being evaluated in Phase 1 clinical trial colorectal cancer (CRC) and other malignancies. Improved pre-clinical understanding of the correlates resistance mechanisms PD human disease relevant context critical to better inform drug combination patient selection strategy. Due limited translatability mouse syngeneic models, establishing more...

10.1158/1538-7445.am2024-6357 article EN Cancer Research 2024-03-22

<div>Abstract<p>Nuclear pore complexes (NPC) are the central mediators of nucleocytoplasmic transport. Increasing evidence shows that many cancer cells have increased numbers NPCs and become addicted to nuclear transport machinery. How reducing NPC affects physiology normal whether it could be exploited for therapies has not been investigated. We report inhibition formation, a process mostly restricted proliferating cells, causes selective cell death, prevents tumor growth,...

10.1158/2159-8290.c.6547931.v1 preprint EN 2023-04-03

<div>Abstract<p>Nuclear pore complexes (NPC) are the central mediators of nucleocytoplasmic transport. Increasing evidence shows that many cancer cells have increased numbers NPCs and become addicted to nuclear transport machinery. How reducing NPC affects physiology normal whether it could be exploited for therapies has not been investigated. We report inhibition formation, a process mostly restricted proliferating cells, causes selective cell death, prevents tumor growth,...

10.1158/2159-8290.c.6547931 preprint EN 2023-04-03
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