Novel inhibitors of the STAT3 signaling pathway: an updated patent review (2014-present)

Feng Wang1, Xin-Yu Cao1, Guo-Qiang Lin1

  • 1The Research Center of Chiral Drugs, Shanghai Frontiers Science Center for Traditional Chinese Medicine Chemical Biology and Innovation Research Institute of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, Xuhui, China.

Abstract

Insights

Signal transducer and activator of transcription 3 (STAT3) inhibitors are promising cancer therapies. This review covers recent advances in STAT3 inhibitor development and structure-activity relationships from patent literature.

Area of Science:

  • Molecular Biology
  • Oncology
  • Medicinal Chemistry

Background:

  • Signal transducer and activator of transcription 3 (STAT3) is a key transcription factor regulating oncogenes.
  • Inhibiting STAT3 activation is a promising cancer therapeutic strategy.
  • Despite extensive research, no STAT3 inhibitors have reached the market.

Purpose of the Study:

  • To review recent advancements in STAT3 inhibitors.
  • To focus on structure-activity relationships (SAR) within patent literature.
  • To cover developments from 2014 to the present.

Main Methods:

  • Comprehensive literature search of patent databases.
  • Analysis of STAT3 inhibitors reported in patents.
  • Evaluation of structure-activity relationships.

Main Results:

  • Numerous STAT3 inhibitors with diverse scaffolds have been developed.
  • Several inhibitors have advanced to clinical trials.
  • Emerging inhibitors exhibit novel mechanisms of action.

Conclusions:

  • Targeting STAT3 remains a vital area for anti-cancer drug development.
  • Challenges include STAT3 pathway complexity and inhibitor drug-like properties.
  • Continued research into novel STAT3 inhibitors is warranted.

Related Concept Videos

The JAK-STAT Signaling Pathway01:20

The JAK-STAT Signaling Pathway

Several cytokine receptors have tightly bound Janus kinase or JAK proteins attached at their cytosolic tail. Small signaling molecules such as cytokines, growth hormones, or prolactins bind to the cytokine receptors and initiate their dimerization. The dimerization brings the cytosolic JAKs together that trans-phosphorylate and activates each other. The activated JAKs now phosphorylate cytosolic tails of the cytokine receptors, which serve as binding sites for adaptor proteins such as  SH2...
9.4K
PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a...
4.1K
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
7.9K
NF-κB-dependent Signaling Pathway02:26

NF-κB-dependent Signaling Pathway

The transcription factor NF-κB was discovered in 1986 in the lab of Nobel laureate Professor David Baltimore, for its interaction with the immunoglobulin light chain enhancer in B-cells. After more than three decades of study, it is now evident that NF-κB regulates the expression of over 100 genes. Most of these genes play an essential role in the innate and adaptive immune responses as well as the inflammatory responses of animals.
NF-κB-dependent Signaling Mechanism
The...
7.9K
Inhibition of Cdk Activity02:34

Inhibition of Cdk Activity

The orderly progression of the cell cycle depends on the activation of Cdk protein by binding to its cyclin partner. However, the cell cycle must be restricted when undergoing abnormal changes. Most cancers correlate to the deregulated cell cycle, and since Cdks are a central component of the cell cycle, Cdk inhibitors are extensively studied to develop anticancer agents. For instance, cyclin D associates with several Cdks, such as Cdk 4/6, to form an active complex. The cyclin D-Cdk4/6 complex...
5.0K
Abnormal Proliferation02:23

Abnormal Proliferation

Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the...
4.7K