LYRM2 directly regulates complex I activity to support tumor growth in colorectal cancer by oxidative phosphorylation

Q Huang, Z Chen, P Cheng, Z Jiang, Z Wang, Y Huang… - Cancer Letters, 2019 - Elsevier
Q Huang, Z Chen, P Cheng, Z Jiang, Z Wang, Y Huang, C Yang, J Pan, F Qiu, J Huang
Cancer Letters, 2019Elsevier
Oxidative phosphorylation (OXPHOS) in cancer has attracted a considerable attention in the
past decades, and accumulated evidence has suggested that it plays an important role in
tumor proliferation, metastasis and drug resistance. However, the mechanisms involved in
these effects are still ambiguous to date. In this study, we found that LYR motif containing 2
(LYRM2), a novel molecule, is up-regulated in colorectal cancer and promotes tumor growth
both in vivo and in vitro. Furthermore, we discovered that LYRM2 locates in the …
Abstract
Oxidative phosphorylation (OXPHOS) in cancer has attracted a considerable attention in the past decades, and accumulated evidence has suggested that it plays an important role in tumor proliferation, metastasis and drug resistance. However, the mechanisms involved in these effects are still ambiguous to date. In this study, we found that LYR motif containing 2 (LYRM2), a novel molecule, is up-regulated in colorectal cancer and promotes tumor growth both in vivo and in vitro. Furthermore, we discovered that LYRM2 locates in the mitochondria, directly interacts with complex I and increases its activity, thus promoting OXPHOS in colorectal cancer cells. More importantly, we identified a new Akt-S58phos-LYRM2-Complex I axis, which is responsible for the LYRM2-induced tumor growth and the activation of OXPHOS in colorectal cancer. Our finding illustrates the role of LYRM2 in regulating tumor metabolism and provides a new potential target for colorectal cancer treatment.
Elsevier