Reassessing the Role of Tissue Factor Pathway Inhibitor 2 in Neoplastic and Non-Neoplastic Lesions

Hiroshi Kobayashi1,2, Hiroshi Shigetomi2,3, Shogo Imanaka1,2

  • 1Department of Gynecology and Reproductive Medicine, Ms. Clinic MayOne, 871-1 Shijo-cho, Kashihara 634-0813, Japan.

Cancers
|May 14, 2025
PubMed
Abstract

Insights

Tissue factor pathway inhibitor 2 (TFPI2) has dual roles in cancer, suppressing tumors but also promoting progression in some. This review explores TFPI2

Area of Science:

  • Oncology
  • Molecular Biology
  • Immunology

Background:

  • Tissue factor pathway inhibitor 2 (TFPI2) is a serine protease inhibitor with known tumor-suppressive functions.
  • TFPI2 promoter hypermethylation often silences its transcription, correlating with increased tumor aggressiveness.
  • Paradoxically, elevated TFPI2 levels are linked to poorer prognosis in ovarian, endometrial, and renal cell carcinomas, indicating a tumor-promoting role in certain cancers.

Purpose of the Study:

  • To review TFPI2 regulation, its downstream targets, and prognostic significance.
  • To re-evaluate TFPI2's role in tumorigenesis, especially in clear cell carcinoma and chronic inflammation.

Main Methods:

  • A comprehensive literature search was conducted using PubMed and Google Scholar.
  • No time restrictions were imposed on the literature search.

Main Results:

  • TFPI2 expression is regulated by transcription factors, signaling molecules, growth factors, cytokines, and epigenetic modifications.
  • TFPI2 influences cell proliferation, inflammation, extracellular matrix remodeling, and vascular cell proliferation within the tumor microenvironment.
  • TFPI2 may modulate transcription factors to affect tumor-associated macrophage (TAM) polarization, potentially facilitating cancer invasion and interacting with inflammatory cells.

Conclusions:

  • TFPI2 plays a role in regulating cell proliferation and inflammation, potentially through interactions with TAMs and inflammatory cells.
  • TFPI2 contributes to maintaining tissue homeostasis but can also influence disease progression in contexts like cancer and chronic inflammation.

Related Concept Videos

Anticoagulant Drugs: Low-Molecular-Weight Heparins01:30

Anticoagulant Drugs: Low-Molecular-Weight Heparins

Hemostasis is a crucial process that prevents excessive blood loss from damaged blood vessels. It involves various mechanisms such as vasoconstriction, platelet adhesion and activation, and fibrin formation. The importance of each mechanism depends on the type of vessel injury. In contrast, thrombosis is the abnormal formation of a blood clot within the blood vessels, leading to potential complications if the clot obstructs blood flow. Thrombosis can be caused by increased coagulability of the...
573
Extrinsic and Intrinsic Pathways of Hemostasis01:20

Extrinsic and Intrinsic Pathways of Hemostasis

Blood clotting or coagulation involves extrinsic and intrinsic pathways, which ultimately merge into the common pathway, forming a fibrin clot.
The Extrinsic Pathway
The extrinsic pathway of coagulation is typically initiated by tissue damage that exposes blood to tissue factor (TF), a protein released by the damaged tissue cells outside the blood vessels—this interaction with TF triggers biochemical reactions involving specific clotting factors. The key player here is Factor VII, which...
4.3K
Cancer-Critical Genes II: Tumor Suppressor Genes01:05

Cancer-Critical Genes II: Tumor Suppressor Genes

Genes usually encode proteins necessary for the proper functioning of a healthy cell. Mutations can often cause changes to the gene expression pattern, thereby altering the phenotype.
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...
7.3K
The Intrinsic Apoptotic Pathway01:31

The Intrinsic Apoptotic Pathway

Internal cellular stress, such as cellular injury or hypoxia, triggers intrinsic apoptosis. The B-cell lymphoma 2 (Bcl-2) family of proteins are the primary regulators of the intrinsic apoptotic pathway. For example, during DNA damage, checkpoint proteins, such as Ataxia Telangiectasia Mutated (ATM protein) and Checkpoints Factor-2 (Chk2) proteins, are activated. These proteins phosphorylate p53 which further activates pro-apoptotic proteins, such as Bax, Bak, PUMA, and Noxa, and inhibits...
5.7K
Regulation of Angiogenesis and Blood Supply01:24

Regulation of Angiogenesis and Blood Supply

Rapidly dividing tumors, embryos, and wounded tissues require more oxygen than usual, lowering the oxygen concentration in the blood. At low oxygen or hypoxic conditions, an oxygen-sensitive transcription factor called the hypoxia-inducible factor 1 or HIF1 is activated. HIF1 is a dimeric protein of alpha (ɑ) and beta (β) subunits.  Under optimal oxygen conditions, HIF1β is present in the nucleus while HIF1ɑ remains in the cytosol. HIF1ɑ is hydroxylated by prolyl...
2.5K
The Tumor Microenvironment02:17

The Tumor Microenvironment

Every normal cell or tissue is embedded in a complex local environment called stroma, consisting of different cell types, a basal membrane, and blood vessels. As normal cells mutate and develop into cancer cells, their local environment also changes to allow cancer progression. The tumor microenvironment (TME) consists of a complex cellular matrix of stromal cells and the developing tumor. The cross-talk between cancer cells and surrounding stromal cells is critical to disrupt normal tissue...
6.5K