Expression Status of Rap1 Pathway-Related Genes in Liver Metastases Compared with Corresponding Primary Colorectal

Maryam Abbastabar1,2, Heike Allgayer3, Mahdi Sepidarkish4

  • 1Student Research Committee, Babol University of Medical Sciences, Babol 47176-47745, Iran.

Cancers
|January 11, 2024
PubMed

Insights

This study investigated Rap1 pathway genes in colorectal cancer liver metastasis (CRLM). NRAS, FGF1, and KDR showed higher expression in metastatic tissues, suggesting their role in metastasis and potential as diagnostic markers.

Area of Science:

  • Molecular biology
  • Oncology
  • Cancer research

Background:

  • Colorectal cancer liver metastasis (CRLM) molecular networks are not fully understood.
  • Identifying molecular drivers of metastasis is crucial for targeted therapies.

Purpose of the Study:

  • To investigate the expression of Rap1 pathway-related genes in CRLM.
  • To evaluate the diagnostic potential of these genes in distinguishing metastatic from non-metastatic colorectal cancer (CRC).

Main Methods:

  • Quantitative real-time PCR (qRT-PCR) and Western blot analysis were used.
  • Gene and protein expression of NRAS, FGF1, NGF, and KDR were assessed.
  • Paired CRC, adjacent noncancerous, and CRLM tissues were analyzed from 30 patients.

Main Results:

  • NRAS, FGF1, and KDR mRNA and protein levels were significantly higher in CRLM tissues compared to primary CRC and adjacent noncancerous tissues (p < 0.05).
  • No significant difference in NRAS, FGF1, KDR, and NGF expression was observed between primary CRC and adjacent noncancerous tissues in non-metastatic patients (p > 0.05).
  • Receiver Operating Characteristic (ROC) curve analysis indicated diagnostic accuracy for NRAS, FGF1, KDR, and FGF in discriminating metastatic from non-metastatic patients based on primary tumor analysis.

Conclusions:

  • The findings suggest that NRAS, FGF1, and KDR play a role in CRLM development.
  • These genes show potential as biomarkers for diagnosing metastasis in colorectal cancer.
  • Further functional studies on Rap1-related genes in CRLM are warranted to advance treatment and prevention strategies.

Related Concept Videos

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...
3.8K
The Ras Gene02:38

The Ras Gene

The Ras-gene-encoded proteins are regulators of signaling pathways controlling cell proliferation, differentiation, or cell survival. The Ras-gene family in humans constitutes three primary members—the HRas, NRas, and KRas. These genes code for four functionally distinct yet closely related proteins—the HRas, NRas, KRas4A, and KRas4B. The involvement of mutant Ras genes in human cancer was first discovered in 1982 and is among the most common causes of human tumorigenesis.
Ras is a...
6.2K
Tumor Progression02:07

Tumor Progression

Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
6.3K
PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a...
3.6K