# The TIP60-CD44 Axis Modulates Colorectal Cancer Stemness

## TL;DR

This study shows that TIP60 influences colorectal cancer stemness by regulating CD44, impacting cancer cell growth and spread.

## Contribution

The study identifies the TIP60-CD44 axis as a novel regulator of colorectal cancer stemness and metastasis.

## Key findings

- TIP60 depletion reduces colorectal cancer cell proliferation and alters colony formation.
- Loss of TIP60 decreases CD44 expression, a key cancer stem cell marker.
- CD44 overexpression reverses the effects of TIP60 depletion on cell proliferation and EMT.

## Abstract

HIV-1 Tat-interactive protein of 60 kDa (TIP60) is a lysine acetyltransferase protein that can acetylate histone and non-histone proteins. This study highlights TIP60’s role in regulating colorectal cancer (CRC) stemness. The depletion of TIP60 resulted in a marked decrease in cellular proliferation, highlighting TIP60’s involvement in the progression of CRC. Additionally, the loss of TIP60 impacted colony formation, transitioning from densely packed structures to dispersed spindle networks along with the loss of E-cadherin, indicating its role in the epithelial–mesenchymal transition (EMT). Three-dimensional culture models suggest that TIP60 is vital for spheroid formation, highlighting its importance in maintaining cancer stem cell properties in CRC. TIP60-depleted cells showed increased invasion in a 3D basement membrane extract (BME) invasion matrix, demonstrating its essential role in cellular invasiveness. Mechanistically, the reduction of TIP60 resulted in a decrease in CD44 expression, a critical marker for cancer stem cells (CSCs). Notably, CD44 overexpression restored the efficiency of spheroid formation and cell proliferation while reversing the EMT phenotype. Developing the TIP60-CD44 axis as a therapeutic target to treat CRC stemness and metastasis will help decrease the burden due to the deadly disease.