Integrated Analysis of the Transcriptome Profile Reveals the Potential Roles Played by Long Noncoding RNAs in

Boran Pang1,2, Yongqiang Hao1,2

  • 1Shanghai Key Laboratory of Orthopaedic Implants, Department of Orthopaedic Surgery, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Frontiers in Oncology
|June 28, 2021
PubMed
Abstract

Insights

Long noncoding RNAs (lncRNAs) drive immune checkpoint inhibitor resistance in sarcoma by promoting immune evasion. Targeting these lncRNAs may improve immunotherapy effectiveness for cancer patients.

Area of Science:

  • Oncology
  • Immunology
  • Genomics

Background:

  • Standard treatments for high-risk soft tissue sarcoma show limited long-term survival.
  • Immune checkpoint inhibitors (ICIs) have shown limited efficacy in sarcoma clinical trials.
  • Identifying resistance mechanisms to ICIs is crucial for improving sarcoma treatment.

Purpose of the Study:

  • To identify key long noncoding RNAs (lncRNAs) associated with immune checkpoint inhibitory molecules in sarcoma.
  • To explore the correlation between lncRNA expression, patient prognosis, and immune evasion.
  • To investigate the potential of lncRNAs as therapeutic targets for overcoming ICI resistance.

Main Methods:

  • Bioinformatic analysis of The Cancer Genome Atlas (TCGA) data.
  • Examination of lncRNA expression levels and their correlation with prognosis.
  • KEGG and GO analysis to determine the functional roles of identified lncRNAs.
  • Analysis of DNA methylation and immune cell infiltration associated with lncRNAs.

Main Results:

  • Upregulated lncRNAs correlated with immune evasion and worse prognosis in sarcoma and other cancers.
  • Low DNA methylation at lncRNA loci was observed, negatively correlating with lncRNA expression.
  • High lncRNA expression was linked to increased suppressive immune cell infiltration and reduced sensitivity to ICIs.

Conclusions:

  • lncRNAs contribute to immune checkpoint inhibitor resistance in human cancers, including sarcoma.
  • These lncRNAs represent potential therapeutic targets for enhancing immunotherapy efficacy.
  • Further research into lncRNA mechanisms can guide novel treatment strategies for immunotherapy resistance.

Related Concept Videos

lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
9.2K
lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

3.1K
Tumor Immunotherapy01:27

Tumor Immunotherapy

Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.
785
Rous Sarcoma Virus (RSV) and Cancer01:03

Rous Sarcoma Virus (RSV) and Cancer

Rous Sarcoma virus or RSV was discovered by F. Peyton Rous in the year 1911 as a filterable transmissible agent that could cause tumors in chickens. He won a Nobel Prize for this discovery in 1966. His experiments clearly demonstrated that some cancers could be caused by infectious agents and led to the discovery of many more cancer-causing viruses in animals as well as humans.
RSV is a retrovirus that contains two copies of a plus-strand  RNA genome. Its genome consists of four main open...
5.6K
MicroRNAs01:22

MicroRNAs

MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
3.3K
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
4.0K