Related Experiment Video
Updated: Jan 13, 2026

Establishment of a Human Multiple Myeloma Xenograft Model in the Chicken to Study Tumor Growth, Invasion and Angiogenesis
Published on: May 1, 2015
[COX6C Promotes the Proliferation of Multiple Myeloma Cells by Increasing Intracellular ATP Levels]
Zhi-Hua Li1, Yi-Hua Wang2, Wen-Hua Liu3
1Department of Hematology, Sinopharm Tongmei General Hospital, Datong 037007, Shanxi Province, China.
Objective:
To investigate the effect of COX6C on the proliferation of multiple myeloma (MM) cells and its mechanism of action.
Methods:
The expression of COX6C in MM cell lines were detected by RT-PCR. siRNA technology was used to knockdown COX6C expression in OPM2 cells. MTT assay and flow cytometry were employed to assess the effect of COX6C knockdown by siRNA on cell proliferation, mitochondrial membrane potential (ΔΨm), and intracellular adenosine triphosphate (ATP) levels. The mitochondrial morphological changes in OPM2 cells pre- and post- siRNA-mediated COX6C knockdown were observed by transmission electron microscopy (TEM).
Results:
The relative expression level of COX6C was significantly increased in MM cell lines (P <0.01). Following siRNA-mediated COX6C knockdown, OPM2 cell proliferation was inhibited, with viable cells accounting for 62.32%±3.43% and 47.01%±5.12% after 48 and 72 hours of culture, respectively. siRNA-mediated COX6C knockdown also caused significant reductions in mitochondrial membrane potential and intracellular ATP levels (P <0.05), accompanied by mitochondrial shortening, swelling, and incomplete cristae structures.
Conclusion:
COX6C may promote the proliferation of MM cells by altering the mitochondrial structure and elevating intracellular ATP levels.
More Related Videos
Related Concept Videos
Abnormal Proliferation
Differentiation of Common Myeloid Progenitor Cells
Adaptive Mechanisms in Cancer Cells
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...
Mitogens and the Cell Cycle
Induced Pluripotent Stem Cells
Somatic...
mTOR Signaling and Cancer Progression
The mTOR pathway or the...

