Related Experiment Video
Updated: Jun 22, 2025

Non-invasive Assessment of the Efficacy of New Therapeutics for Intestinal Pathologies Using Serial Endoscopic Imaging of Live Mice
Published on: March 10, 2015
Arachidonic acid metabolism as a novel pathogenic factor in gastrointestinal cancers
Weiqin Lu1, Aihemaitijiang Aihaiti2, Paziliya Abudukeranmu2
1General Surgery, Cancer Center, Department of Vascular Surgery, Zhejiang Provincial People's Hospital (Affiliated People's Hospital), Hangzhou Medical College, Hangzhou, Zhejiang, China.
Abstract:
Gastrointestinal (GI) cancers are a major global health burden, representing 20% of all cancer diagnoses and 22.5% of global cancer-related deaths. Their aggressive nature and resistance to treatment pose a significant challenge, with late-stage survival rates below 15% at five years. Therefore, there is an urgent need to delve deeper into the mechanisms of gastrointestinal cancer progression and optimize treatment strategies. Increasing evidence highlights the active involvement of abnormal arachidonic acid (AA) metabolism in various cancers. AA is a fatty acid mainly metabolized into diverse bioactive compounds by three enzymes: cyclooxygenase, lipoxygenase, and cytochrome P450 enzymes. Abnormal AA metabolism and altered levels of its metabolites may play a pivotal role in the development of GI cancers. However, the underlying mechanisms remain unclear. This review highlights a unique perspective by focusing on the abnormal metabolism of AA and its involvement in GI cancers. We summarize the latest advancements in understanding AA metabolism in GI cancers, outlining changes in AA levels and their potential role in liver, colorectal, pancreatic, esophageal, gastric, and gallbladder cancers. Moreover, we also explore the potential of targeting abnormal AA metabolism for future therapies, considering the current need to explore AA metabolism in GI cancers and outlining promising avenues for further research. Ultimately, such investigations aim to improve treatment options for patients with GI cancers and pave the way for better cancer management in this area.
Insights
Abnormal arachidonic acid (AA) metabolism is implicated in gastrointestinal (GI) cancers. Understanding these changes could lead to new therapeutic strategies for GI cancer treatment.
Area of Science:
- Oncology
- Biochemistry
- Molecular Biology
Background:
- Gastrointestinal (GI) cancers represent a significant global health challenge, causing substantial mortality.
- Late-stage GI cancers exhibit poor survival rates, necessitating improved treatment strategies.
- Aberrant arachidonic acid (AA) metabolism is increasingly recognized in cancer development.
Purpose of the Study:
- To review the role of abnormal arachidonic acid (AA) metabolism in the progression of GI cancers.
- To summarize current knowledge on AA metabolism alterations in various GI malignancies.
- To explore the therapeutic potential of targeting AA metabolism in GI cancer treatment.
Main Methods:
- Literature review focusing on studies investigating arachidonic acid (AA) metabolism in GI cancers.
- Synthesis of findings on altered AA levels and their metabolites across different GI cancer types.
- Analysis of potential therapeutic targets within the AA metabolic pathway.
Main Results:
- Abnormal arachidonic acid (AA) metabolism is linked to liver, colorectal, pancreatic, esophageal, gastric, and gallbladder cancers.
- Specific changes in AA levels and its metabolites are observed in these GI malignancies.
- The enzymes involved in AA metabolism (COX, LOX, CYP450) are potential targets.
Conclusions:
- Altered arachidonic acid (AA) metabolism is a key factor in GI cancer development and progression.
- Targeting AA metabolic pathways offers a promising avenue for novel GI cancer therapies.
- Further research into AA metabolism is crucial for advancing GI cancer management.
More Related Videos
Related Concept Videos
Pathophysiology of Peptic Ulcer Disease: Injurious Factors
In the antrum region, G cells secrete the gastrin hormone that binds to gastrin-cholecystokinin-B (CCK2) receptors on parietal and enterochromaffin-like (ECL) cells in the fundic glands. Simultaneously, the vagus nerve releases acetylcholine, which binds...
Gastritis-II: Pathophysiology
In acute gastritis, the gastric mucosa becomes swollen and red and undergoes superficial erosion. Superficial ulceration may lead to bleeding.
In chronic gastritis, persistent or repeated insults lead to chronic inflammatory changes and, eventually, thinning or atrophy of the gastric tissue.
Gastritis can stem from various causes, each...
Pathophysiology of Peptic Ulcer Disease: Mucosal Defense Factors
Cancer Cell Migration through Invadopodia
Peptic Ulcer Disease I: Introduction
An acute ulcer, marked by superficial erosion and minimal inflammation, swiftly resolves upon identifying and addressing the underlying cause. In contrast, a chronic ulcer persists, potentially eroding through the muscular wall and forming fibrous tissue.
Peptic ulcers can also be...
IP3/DAG Signaling Pathway

