Technology Overview

Penetration of anti‐tumor therapies is often limited by the tumor microenvironment, which can include a high density of extracellular matrix as well as elevated interstitial fluid pressure, both of which create a barrier to distribution. It is well established that limited intratumoral distribution of anti‐tumor agents leads to sub‐optimal efficacy.

The compositions disclosed here by University at Buffalo researchers enable improved uptake and distribution of anticancer agents, including mAbs and ADCs, with lessened concerns for toxicity due to the presence of targeting domains in combination with the matrix‐modulating enzyme (MME).

In a tumor xenograft model, when trastuzumab was administered following a dose of an untargeted MME, its distribution away from vasculature (red) was limited relative to its administration following a dose of a targeted matrix‐modulating enzyme (TMME) (data not shown). As observed in an example using a trastuzumab‐based ADC (), the increased distribution of the ADC following administration of a TMME translated to an increase in survival compared to the ADC administered alone or following administration of an untargeted MME and both the TMME (alone) and control. These TMMEs can be used in combination with other anticancer therapies to improve their efficacy.

Published in Thesis Dissertation (Chapter 5): https://www.proquest.com/pqdtglobal/docview/2417300634/1128520C22B743BAPQ/3?accountid=14169

Applications

Oncology ‑ solid tumors

Opportunity

Technology available for licensing.

Targeted Matrix-Modulating Enzymes

Patents

IP Status

Seeking