The ERK5/NF-kappa B signaling pathway targets endometrial cancer proliferation and survival


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Dieguez-Martinez N., Espinosa-Gil S., Yoldi G., Megias-Roda E., Bolinaga-Ayala I., Vinas-Casas M., ...More

CELLULAR AND MOLECULAR LIFE SCIENCES, vol.79, no.10, 2022 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 79 Issue: 10
  • Publication Date: 2022
  • Doi Number: 10.1007/s00018-022-04541-6
  • Journal Name: CELLULAR AND MOLECULAR LIFE SCIENCES
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Agricultural & Environmental Science Database, CAB Abstracts, Chemical Abstracts Core, Chimica, EMBASE, MEDLINE, Veterinary Science Database
  • Keywords: Map kinase, ERK5, NF-kB, Apoptosis, Endometrial cancer, Anticancer drug, NF-KAPPA-B, REGULATED KINASE-5, BREAST-CANCER, ERK5, EXPRESSION, GROWTH, CELLS, AMPLIFICATION, ACTIVATION, BMK1/ERK5
  • Van Yüzüncü Yıl University Affiliated: Yes

Abstract

Endometrial cancer (EC) is the most common type of gynecologic cancer in women of developed countries. Despite surgery combined with chemo-/radiotherapy regimens, overall survival of patients with high-risk EC tumors is poor, indicating a need for novel therapies. The MEK5-ERK5 pathway is activated in response to growth factors and to different stressors, including oxidative stress and cytokines. Previous evidence supports a role for the MEK5-ERK5 pathway in the pathology of several cancers. We investigated the role of ERK5 in EC. In silico analysis of the PanCancer Atlas dataset showed alterations in components of the MEK5-ERK5 pathway in 48% of EC patients. Here, we show that ERK5 inhibition or silencing decreased EGF-induced EC cell proliferation, and that genetic deletion of MEK5 resulted in EC impaired proliferation and reduced tumor growth capacity in nude mice. Pharmacologic inhibition or ERK5 silencing impaired NF-kB pathway in EC cells and xenografts. Furthermore, we found a positive correlation between ERK5 and p65/RELA protein levels in human EC tumor samples. Mechanistically, genetic or pharmacologic impairment of ERK5 resulted in downregulation of NEMO/IKK gamma expression, leading to impaired p65/RELA activity and to apoptosis in EC cells and xenografts, which was rescued by NEMO/IKK gamma overexpression. Notably, ERK5 inhibition, MEK5 deletion or NF-kB inhibition sensitized EC cells to standard EC chemotherapy (paclitaxel/carboplatin) toxicity, whereas ERK5 inhibition synergized with paclitaxel to reduce tumor xenograft growth in mice. Together, our results suggest that the ERK5-NEMO-NF-kappa B pathway mediates EC cell proliferation and survival. We propose the ERK5/NF-kappa B axis as new target for EC treatment.