@imperialsandc.bsky.social | @imperialcollegeldn.bsky.social
profiles.imperial.ac.uk/p.leung
Huge thanks to the team: Innah, Bibek @ogsurgery.bsky.social, @hannagroupicl.bsky.social
@imperialsandc.bsky.social @imperialmed.bsky.social @imperialcollegeldn.bsky.social
Read the full open access study here: www.nature.com/articles/s41...
Double celebration day: PhD graduation + paper🥂
Huge thanks to the team: Innah, Bibek @ogsurgery.bsky.social, @hannagroupicl.bsky.social
@imperialsandc.bsky.social @imperialmed.bsky.social @imperialcollegeldn.bsky.social
Read the full open access study here: www.nature.com/articles/s41...
Double celebration day: PhD graduation + paper🥂
This supports VOCs as surrogate readouts of therapy-altered lipid metabolism.
Why this matters:
This small piece of work demonstrates the potential of VOCs in breath or biofluids as real-time biomarkers for monitoring treatment response in precision oncology.
This supports VOCs as surrogate readouts of therapy-altered lipid metabolism.
Why this matters:
This small piece of work demonstrates the potential of VOCs in breath or biofluids as real-time biomarkers for monitoring treatment response in precision oncology.
To validate, we oxidised lipid standards → VOCs were only generated from unsaturated lipids, and traceable back to double bond breakages in fatty acids.
Multi-omics integration (DIABLO) revealed strong VOC–lipid correlations (r > 0.7).
To validate, we oxidised lipid standards → VOCs were only generated from unsaturated lipids, and traceable back to double bond breakages in fatty acids.
Multi-omics integration (DIABLO) revealed strong VOC–lipid correlations (r > 0.7).
What we found:
Resistant cells released unique VOCs post-treatment:
Alkenes, Aldehydes (e.g. hexanal, nonanal), short chain fatty acids (e.g. nonanoic, 5-octenoic acid)
These VOCs correlated with lipid species rich in oleic, linoleic, and arachidonic acid.
What we found:
Resistant cells released unique VOCs post-treatment:
Alkenes, Aldehydes (e.g. hexanal, nonanal), short chain fatty acids (e.g. nonanoic, 5-octenoic acid)
These VOCs correlated with lipid species rich in oleic, linoleic, and arachidonic acid.
What we did:
mTORi-sensitive and -resistant CRC cell lines
Treated with OSI-027/AZD2014
Paired untargeted LC-MS lipidomics + GC-MS volatilomics
What we did:
mTORi-sensitive and -resistant CRC cell lines
Treated with OSI-027/AZD2014
Paired untargeted LC-MS lipidomics + GC-MS volatilomics
Why mTOR?
mTOR regulates lipid biosynthesis and is often dysregulated in colorectal cancer.
We hypothesised that mTOR inhibitor–resistant cells would exhibit a distinct lipidomic and volatilomic profile compared to sensitive ones.
Why mTOR?
mTOR regulates lipid biosynthesis and is often dysregulated in colorectal cancer.
We hypothesised that mTOR inhibitor–resistant cells would exhibit a distinct lipidomic and volatilomic profile compared to sensitive ones.
🌬️ VOCs = volatile organic compounds
These are carbon-based molecules produced by cells, which are detectable in breath, urine, and other biofluids.
They're safe, easy to sample, and can reflect underlying metabolic shifts, particularly in lipid metabolism.
🌬️ VOCs = volatile organic compounds
These are carbon-based molecules produced by cells, which are detectable in breath, urine, and other biofluids.
They're safe, easy to sample, and can reflect underlying metabolic shifts, particularly in lipid metabolism.
🎯 The challenge:
Targeted cancer therapies like mTOR inhibitors often show variable patient responses.
We urgently need non-invasive, repeatable, and real-time biomarkers to track treatment response.
Could VOCs be the answer?
🎯 The challenge:
Targeted cancer therapies like mTOR inhibitors often show variable patient responses.
We urgently need non-invasive, repeatable, and real-time biomarkers to track treatment response.
Could VOCs be the answer?
for a fantastic discussion and their valuable feedback.
My PhD explored the effects of intra-tumoural acidity on lipid metabolism and volatile biomarker production in oesophageal adenocarcinoma.
for a fantastic discussion and their valuable feedback.
My PhD explored the effects of intra-tumoural acidity on lipid metabolism and volatile biomarker production in oesophageal adenocarcinoma.