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Network Analysis of Foramen Ovale Electrode Recordings in Drug-resistant Temporal Lobe Epilepsy Patients
Published on: December 18, 2016
Long-range and short-range tumor-stroma networks synergistically contribute to tumor-associated epilepsy
Xiao-Yuan Mao1,2, Tursonjan Tokay3, Hong-Hao Zhou1,2
1Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, P. R. China.
Abstract:
Epileptic seizures are frequently caused by brain tumors. Traditional anti-epileptic treatments do not acquire satisfactory responses. Preoperative and postoperative seizures seriously influence the quality of life of patients. Thus, tumor-associated epilepsy (TAE) is an important subject of the current research. The delineation of the etiology of epileptogenesis in patients with primary brain tumor may help to find the novel and effective drug targets for treating this disease. In this review, we describe the current status of treatment of TAE. More importantly, we focus on the factors that are involved in the functional connectivity between tumors and stromal cells. We propose that there exist two modes, namely, long-range and short-range modes, which likely trigger neuronal hyperexcitation and subsequent epileptic seizures. The long-range mode is referred to as factors released by tumors including glutamate and GABA, binding to the corresponding receptor on the cellular membrane and causing neuronal hyperactivity, while the short-range mode is considered to involve direct intracellular communication between tumor cells and stromas. Gap junctions and tunneling nanotube network are involved in cellular interconnections. Future investigations focused on those two modes may find a potential novel therapeutic target for treating TAE.
Insights
Tumor-associated epilepsy (TAE) involves seizures linked to brain tumors, often resistant to standard treatments. Understanding tumor-stromal cell interactions may reveal new therapeutic targets for seizure control.
Area of Science:
- Neuroscience
- Oncology
- Pharmacology
Background:
- Epileptic seizures are a common complication of brain tumors, significantly impacting patient quality of life.
- Existing anti-epileptic treatments often provide inadequate responses for tumor-associated epilepsy (TAE).
- Investigating the mechanisms of epileptogenesis in TAE is crucial for developing effective therapies.
Purpose of the Study:
- To review the current treatment landscape for TAE.
- To explore the functional connectivity between brain tumors and stromal cells in the context of epileptogenesis.
- To propose novel therapeutic targets based on identified interaction modes.
Main Methods:
- Literature review focusing on TAE treatments and underlying mechanisms.
- Analysis of factors contributing to functional connectivity between tumor and stromal cells.
- Identification and categorization of proposed interaction modes (long-range and short-range).
Main Results:
- Two primary modes of tumor-stromal cell interaction are proposed: long-range and short-range.
- The long-range mode involves tumor-secreted factors (e.g., glutamate, GABA) causing neuronal hyperexcitation.
- The short-range mode involves direct intercellular communication via gap junctions and tunneling nanotubes.
Conclusions:
- Understanding these long-range and short-range interaction modes is key to elucidating TAE pathogenesis.
- Targeting these specific communication pathways could lead to novel therapeutic strategies for TAE.
- Further research into these mechanisms holds promise for improved seizure management in brain tumor patients.
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