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University of Houston

A Structure-Activity Relationship Study with Isoquinolinone Compounds and Stromal Antigen 2 Mutant Ewing’s Sarcoma Cells and Synthesis of Small Molecules for Anticancer Activity Through TEAD Palmitoylation Inhibition

Abstract

dc:description.abstract

There are two distinct projects that will be discussed in this dissertation. The first section will be focused on the structure-activity relationship study with isoquinolinone compounds, and the second on the synthetic approach to small molecules that inhibit the growth of cancer cells through the Hippo signaling pathway. Ewing’s sarcoma is the second most commonly diagnosed pediatric bone cancer. While there are common forms of general treatment available, there are little to no treatments for recurrent cases, as well as malignant tumors. Our collaborators at the Baylor College of Medicine found in a high throughput screening an isoquinolinone compound, StagX1, which is selectively active in inhibiting and decreasing the cell viability of STAG 2 mutant cancer cells in an environment of wild type cancer cells. SAR studies have been performed to find new derivatives with increased the efficacy, general solubility, and plasma stability. Different delivery systems, such as liposomes, have been implemented to help identify the true active compound towards the cancer cell lines. The Hippo signaling pathway is a cell signaling pathway that was recently linked to cancer development and immunotherapy. Mutation or malfunction in the signaling pathway leads to irregular cell growth, especially in the case of tumor cells. To support cell regulation and prevent cancer cell proliferation, the TEAD protein is prohibited from undergoing palmitoylation, in which cell proliferation and anti-apoptosis is prevented. Two small hydrophobic structures were discovered through virtual ligand screening by our collaborators. Two initial synthetic routes were completed to initiate efficient production of products and further advancement in biological and SAR studies.

Degree

thesis:*
Name thesis:degree_name
Doctor of Philosophy
Level thesis:degree_level
Doctoral
Discipline thesis:degree_discipline
Chemistry
Grantor
University of Houston
Year dc:date.issued
2023

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Yang, Christian
Advisor dc:contributor.advisor
  • Gilbertson, Scott R.
Committee members dc:contributor.committeemember
  • Lee, T. Randall
  • Comito, Robert J.
  • Chen, Tai-Yen
  • Pati, Debananda

Subjects

dc:subject × 1

Rights

dc:rights
Statement dc:rights
  • The author of this work is the copyright owner. UH Libraries and the Texas Digital Library have their permission to store and provide access to this work. Further transmission, reproduction, or presentation of this work is prohibited except with permission of the author(s).
Language dc:language.iso
eng

Identifiers

dc:identifier.*
Handle dc:identifier.uri
https://hdl.handle.net/10657/14541
OAI identifier oai:identifier
oai:uh-ir.tdl.org:10657/14541

Chain of custody

source
Harvested from
University of Houston
Base URL
uh-ir.tdl.org/server/oai/request
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Yang, Christian. A Structure-Activity Relationship Study with Isoquinolinone Compounds and Stromal Antigen 2 Mutant Ewing’s Sarcoma Cells and Synthesis of Small Molecules for Anticancer Activity Through TEAD Palmitoylation Inhibition. Doctoral thesis, University of Houston, 2023. https://hdl.handle.net/10657/14541