# lncRNA NKILA Promotes Warburg Effect and Immune Escape in Intrahepatic Cholangiocarcinoma by Regulating the MTX1/TOMM40 Axis

## TL;DR

The lncRNA NKILA promotes cancer growth and immune evasion in intrahepatic cholangiocarcinoma by regulating the MTX1/TOMM40 axis.

## Contribution

This study identifies a novel regulatory mechanism involving NKILA in promoting tumor progression and immune escape in intrahepatic cholangiocarcinoma.

## Key findings

- NKILA, MTX1, and TOMM40 are upregulated in ICC tissues and NKILA silencing reduces MTX1-TOMM40 binding.
- NKILA promotes ICC cell proliferation, invasion, Warburg effect, and autophagy by regulating the mTOR pathway and PD-L1 expression.
- NKILA binds to MTX1 mRNA, stabilizing it and promoting MTX1 protein expression, which is essential for the observed effects.

## Abstract

Intrahepatic cholangiocarcinoma (ICC) is an aggressive malignancy with high heterogeneity and poor prognosis. Long noncoding RNAs (lncRNAs) play critical roles in tumorigenesis through dysregulated expression. We explored the effects and mechanisms of nuclear transcription factor NF‐κB interacting lncRNA (NKILA) in ICC.

Bioinformatic analysis was performed to determine the expression and relationship of NKILA with metaxin 1 (MTX1), and translocase of outer mitochondrial membrane 40 (TOMM40) expression in ICC tissue samples. Cholangiocarcinoma cell lines were cultured in vitro and the transplanted tumor model was constructed in vivo to study the role of NKILA in ICC. Immunohistochemistry (IHC), Western blot, and quantitative real‐time polymerase chain reaction (qRT‐PCR) were used to detect the effects of NKILA on the Warburg effect, autophagy, programed cell death 1 ligand 1 (PD‐L1) expression, and CD8+ T cytotoxicity in ICC cells. RNA immunoprecipitation (IP) (RIP) assay and RNA–RNA pull down assays were utilized to detect the binding of NKILA and MTX1, and CO‐IP was performed to assess the interaction between MTX1 and TOMM40.

We found that NKILA, MTX1, and TOMM40 were substantially upregulated in ICC tissues, and NKILA silencing reduced MTX1‐TOMM40 binding in ICC cells. NKILA facilitated proliferation, invasion, Warburg effects, and autophagy of ICC cells by regulating mammalian target of rapamycin (mTOR) pathway, PD‐L1 expression, and CD8+ T cytotoxicity, while dichloroacetate (DCA) could reverse these effects. Mechanistically, NKILA binds directly to MTX1 mRNA, which stabilizes MTX1 mRNA and thereby promotes the expression of MTX1 protein. NKILA silencing could inactivate MTX1/TOMM40 axis to inhibit Warburg effect and autophagy‐associated immune escape.

LncRNA NKILA promotes Warburg effect and immune escape in ICC by regulating the MTX1/TOMM40 axis.