Fibulin-3 sponges Tiam1 to manipulate MMP-7 activity through β-catenin signaling in oral squamous cell carcinoma

Honglei Guo1, Yangyang Ji2, Bo Zhang3

  • 1School and Hospital of Stomatology, Tianjin Medical University, Tianjin, China.

Insights

T-lymphoma invasion and metastasis inducing factor 1 (Tiam1) drives oral squamous cell carcinoma (OSCC) progression by promoting epithelial-mesenchymal transition. Tiam1 competes with Fibulin-3 for nuclear β-catenin, activating MMP-7 and aiding OSCC development.

Area of Science:

  • Oncology
  • Molecular Biology
  • Cell Biology

Background:

  • Oral squamous cell carcinoma (OSCC) is a prevalent malignancy with an unclear molecular basis.
  • T-lymphoma invasion and metastasis inducing factor 1 (Tiam1) is a potential oncogene in OSCC.

Purpose of the Study:

  • To elucidate the signaling mechanism of Tiam1 in oral squamous cell carcinoma (OSCC) progression.
  • To investigate the interplay between Tiam1, Fibulin-3, and MMP-7 in OSCC development.

Main Methods:

  • RT-PCR and ELISA were used to measure gene and protein expression in OSCC patients.
  • Luciferase reporter assays and western blotting were performed on the CAL27 cell line.
  • Analysis included gene transfection, protein marker examination, and interaction studies.

Main Results:

  • Fibulin-3 expression decreased with increasing TNM stage, while Tiam1 and MMP-7 levels increased.
  • Tiam1 promoted MMP-7 expression via β-catenin nuclear translocation, opposing Fibulin-3's function.
  • Tiam1 directly interacted with Fibulin-3, inducing OSCC epithelial-mesenchymal transition (EMT) through MMP-7 activation.

Conclusions:

  • Tiam1 competes with Fibulin-3 for nuclear β-catenin, activating MMP-7 and initiating EMT in OSCC.
  • This study proposes a novel signaling pathway involving Tiam1, Fibulin-3, β-catenin, and MMP-7 in OSCC progression.
  • Findings offer insights for future clinical studies on OSCC treatment.

Related Concept Videos

Role of Matrix Metalloproteases in Degradation of ECM01:23

Role of Matrix Metalloproteases in Degradation of ECM

Matrix metalloproteases (MMPs) are enzymes involved in the hydrolysis of proteins and glycoproteins of the extracellular matrix. MMPs are essential for the migration and proliferation of cells through the dense matrix network, throughout embryonic development, and throughout morphogenesis. The first MMP activity discovered was a collagenase in a tadpole's tail undergoing metamorphosis. The active collagen deposition and modifications lead to the morphogenesis of tadpoles into the adult...
2.5K
Intracellular Signaling Affects Focal Adhesions01:17

Intracellular Signaling Affects Focal Adhesions

Integrins act both as extracellular input receivers and as intracellular processing activators. As their name suggests, integrins are entirely integrated into the membrane structure. Their hydrophobic membrane-spanning regions interact with the phospholipid bilayer's hydrophobic region. These membrane receptors provide extracellular attachment sites for effectors like hormones and growth factors. They activate intracellular response cascades when their effectors are bound and active.
Some...
2.8K
Cancer Cell Migration through Invadopodia01:35

Cancer Cell Migration through Invadopodia

Invadosome is a broad category of cell surface structures with proteolytic activity that  degrades the extracellular matrix (ECM). Invadosomes are present in normal cell types, including macrophages, endothelial cells, and neurons, as well as tumor cells. Although the macrophage podosomes and tumor cell invadopodia are classified as invadosomes, they have different structures, molecular pathways, and functions. Podosomes are short structures that last for a few minutes. However,...
2.4K
Structural Protein Function01:56

Structural Protein Function

Structural proteins are a category of proteins responsible for functions ranging from cell shape and movement to providing support to major structures such as bones, cartilage, hair, and muscles. This group includes proteins such as collagen, actin, myosin, and keratin.
Collagen, the most abundant protein in mammals, is found throughout the body. In connective tissue, such as skin, ligaments, and tendons, it provides tensile strength and elasticity.  In bones and teeth, it mineralizes to...
28.2K
Actin Filament Depolymerization01:19

Actin Filament Depolymerization

Actin filaments (F-actin) are composed of actin subunits. The dissociation of actin monomers can occur from either end of F-actin. The rate of dissociation is faster from the minus-end or the pointed end, where the actin subunits exist with a bound ADP, together known as ADP-actin. The depolymerization of F-actin is aided by proteins, including the actin-depolymerizing factor (ADF) and cofilin family of proteins, gelsolin, and glia maturation factor (GMF).
In F-actin, the ADF/cofilin proteins...
3.2K
Mechanism of Filopodia Formation01:39

Mechanism of Filopodia Formation

Filopodia are thin, actin-rich cellular protrusions that play an important role in many fundamental cellular functions. They vary in their occurrence, length, and positioning in different cell types, suggesting their diverse roles.
Their main function is to guide migrating cells during normal tissue morphogenesis or cancer metastasis by recognizing and making initial contacts with the extracellular matrix. However, they can also act as stationary cell anchors or help to establish communication...
2.5K