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Table 1 Role of plasmalemmal Ca 2+ channels in cell migration and tumor metastasis

From: Remodeling of calcium signaling in tumor progression

Ca2+channel

Cell type

Mechanisms and effectors

References

Store-dependent SOC channels

STIM1-Orai1

• Human cervical cancer SiHa and CaSki cells

• Increase in EGF-stimulated cellular migration and invasion

[29, 30]

• Increase in focal adhesion dynamics through the Ca2+-regulated protease calpain and cytoplasmic kinase Pyk2

• Upregulation of EGF-induced MLC phosphorylation and actomyosin reorganization

• Upregulation of VEGF production

• Promotion of tumor growth and angiogenesis in a xenograft mice model

 

• Human breast cancer MDA-MB-231 cells and mouse mammary tumor 4 T1 cells

• Increase in serum-induced cellular migration and invasion

[31]

• Increase in focal adhesion turnover rates through Ras and Rac1

• Promotion of tumor growth and metastasis in a xenograft mice model

STIM-Orai3

• Human breast cancer MCF7 cells (ER+ breast cancer cells)

• Increase in anchorage-independent growth and Matrigel invasion

[32, 33]

  

• Increase in tumorigenesis in a xenograft mice model

 

Store-independent SOC channel

SPCA2-Orai1

• Human breast cancer MCF-7 cells

• Constitutively active store-independent Ca2+ influx

[34]

• Promotion of proliferation and colony formation

  

• Increase in tumorigenesis in a xenograft mice model

 

TRP channels

TRPM1

• Murine melanoma B16-F1 cells

• Reduce in tumor metastasis

[35, 36]

TRPM7

• Human breast cancer MDA-MB-231 cells and MEF cells

• Increase in cellular migration

[18, 37–39]

• Guidance of polarized cellular migration

• Increase in peripheral focal adhesion turnovers through the Ca2+-regulated protease m-calpain

• Inhibition of myosin II-based cell contractility

• Increase in tumorigenesis in a xenograft mice model

 

• Human nasopharyngeal cancer 5-8 F and 6-10B cells

• Increase in cellular migration

[40]

 

• Human lung cancer A549 cells

• Increase in EGF-stimulated cellular migration

[38]

TRPM8

• Human prostate cancer PC-3 cells

• Decrease in cellular migration

[41, 42]

• Inactivation of FAK

TRPV1

• Human hepatoblastoma HepG2 cells

• Increase in HGF-stimulated cellular migration

[43, 44]

TRPV2

• Human prostate cancer LNCaP and PC-3 cells

• Increase in cellular migration and invasion

[45]

• Induction of invasive enzymes MMP-2, MMP-9 and cathepsin B

• Increase in tumorigenesis in a xenograft mice model

TRPC6

• Human glioblastoma cells

• Increase in cell proliferation through regulation of CDK1 activation and Cdc25C expression

[46, 47]

• Increase in anchorage-independent growth and Matrigel invasion

• Increase in endothelial cell tube formation

  

• Increase in tumorigenesis in a xenograft mice model

 
  1. Cdc25C, cell division cycle 25 homolog C; CDK1, cyclin-dependent kinase 1; EGF, epidermal growth factor; ER, estrogen receptor; FAK, focal adhesion kincase; HGF, hepatocyte growth factor; SPCA2, secretory pathway Ca2+-ATPase; MEF, mouse embryonic fibroblast; MMP, matrix metalloproteinase; Pyk2, proline-rich tyrosine kinase 2; VEGF, vascular endothelial cell growth factor.