The lab is looking to expand! Postdoc applicants and rotation students welcome!

We are looking to expand our lab team! With new anticipated funding in 2021, multiple positions are open to study metabolism, epigenetics, and senescence in cancer. We support both scientific and professional development and foster a diverse and inclusive lab environment. For more information, see: https://airdlab.com/positions.

Email Dr. Aird with a cover letter and CV if interested.

DoD Ovarian Cancer Research Program grant recommended for funding!

We are thrilled that our DoD Ovarian Cancer Research Program Teal Expansion Award application was recommended for funding. This project will expand on Daniel’s finding that ATM inhibition increases tumor cell branched chain amino acid uptake via macropinocytosis. We are even going to do some immunology (in collaboration with Dr. Greg Delgoffe)! We are grateful for this opportunity to learn more about ovarian cancer and how to treat it.

Daniel's ATM inhibitor + fenofibrate paper accepted!

Congratulations to Daniel and co-authors Raquel, Erika, and Kelly for the acceptance of this pandemic-derived paper! Daniel had an interesting observation that ATM status corresponds to metabolic gene signatures, and inhibition of ATM in high grade serous ovarian cancer (usually ATM wildtype) synergizes with the FDA-approved metabolic drug fenofibrate.

Raquel's preprint on p16's regulation of the SASP posted to bioRxiv!

Congrats to Raquel for getting this small paper out the door during these hard times. She found that p16 loss decreases IL6 and IL8 (two of the main effectors of the SASP), which is uncoupled from its role in the cell cycle. These studies have potential implications for understanding the tumor microenvironment of p16-low tumors, and we are planning to do more studies in the area with our new immunology colleagues at Pitt. Read the preprint here: https://www.biorxiv.org/content/10.1101/2020.08.19.257717v1

Congratulations to Daniel for submitting his paper on macropinocytosis!

Hats off to Daniel, who submitted his first paper from the lab today. He found that inhibition of ATM induces nutrient uptake via macropinocytosis- a non-specific endocytic process. This discovery adds to growing evidence that ATM has tumor suppressive roles outside of the canonical DNA damage response pathway. You can read the preprint here.