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Updated: Feb 10, 2026

Isolation of Human Myoblasts, Assessment of Myogenic Differentiation, and Store-operated Calcium Entry Measurement
Published on: July 26, 2017
The store-operated Ca(2+) entry-mediated signaling is important for cancer spread
Yih-Fung Chen1, Keng-Fu Hsu2, Meng-Ru Shen3
1Graduate Institute of Natural Products, College of Pharmacy, Kaohsiung Medical University, Kaohsiung, Taiwan; Center for Research Resources and Development, Kaohsiung Medical University, Kaohsiung, Taiwan; Department of Pharmacology, National Cheng Kung University, Tainan, Taiwan.
Abstract:
Tumor cell migration and invasion are essential steps in the metastatic cascade that has great impact on patient outcomes. Spatial and temporal organization of Ca(2+) signaling regulates the multiple aspects of migration machinery, including cytoskeletal reorganization, traction force generation, and focal adhesion dynamics. Stromal interaction molecules (STIM) and Orai proteins, recently identified as critical constituents of store-operated Ca(2+) entry (SOCE), have been implicated in cancer cell migration and tumor metastasis. The clinical significance of STIM proteins and Orai Ca(2+) channels in tumor progression and their diagnostic and prognostic potentials have also been demonstrated in different types of cancers. Here we review the recent advances in understanding the important roles and regulatory mechanisms of STIM/Orai-mediated SOCE in cancer spread. The clinical implications and the emergence as a selective target for cancer therapeutics are also discussed. This article is part of a Special Issue entitled: Calcium and Cell Fate. Guest Editors: Jacques Haiech, Claus Heizmann, Joachim Krebs, Thierry Capiod and Olivier Mignen.
Insights
Stromal interaction molecules (STIM) and Orai proteins regulate calcium signaling, impacting cancer cell migration and metastasis. Targeting these store-operated calcium entry (SOCE) pathways offers potential for novel cancer therapeutics.
Area of Science:
- Cellular Biology
- Cancer Research
- Molecular Medicine
Background:
- Tumor cell migration and invasion are critical steps in metastasis, significantly affecting patient prognosis.
- Calcium (Ca2+) signaling dynamics are crucial for regulating cell migration processes, including cytoskeletal changes and focal adhesion.
- Stromal interaction molecules (STIM) and Orai proteins are key components of store-operated calcium entry (SOCE), a vital calcium influx pathway.
Purpose of the Study:
- To review recent advancements in understanding the role of STIM/Orai-mediated SOCE in cancer cell migration and metastasis.
- To discuss the regulatory mechanisms governing STIM/Orai function in cancer spread.
- To explore the clinical significance, diagnostic/prognostic potential, and therapeutic implications of targeting STIM/Orai in cancer.
Main Methods:
- Literature review of recent research on STIM/Orai proteins and calcium signaling in cancer.
- Analysis of studies investigating the link between SOCE and tumor progression.
- Examination of clinical data and therapeutic strategies related to STIM/Orai pathways.
Main Results:
- STIM and Orai proteins play significant roles in regulating cancer cell migration and invasion.
- STIM/Orai-mediated SOCE is implicated in various aspects of the metastatic cascade.
- The clinical significance of STIM/Orai in tumor progression and their potential as biomarkers have been demonstrated.
Conclusions:
- STIM/Orai-mediated SOCE is a critical regulator of cancer cell metastasis.
- Understanding these pathways provides insights into tumor progression.
- Targeting STIM/Orai represents a promising therapeutic strategy for cancer treatment.
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