# Low Expression of FAM96B is Associated with Poor Prognosis in Hepatocellular Carcinoma

**Authors:** Yuqun Tang, Liangke Tang, Haijian Du, Chaosheng Wu, Zhuangxiong Wang, Guanshui Luo, Ke He

PMC · DOI: 10.5152/tjg.2024.24198 · The Turkish Journal of Gastroenterology · 2024-12-16

## TL;DR

Low levels of FAM96B in liver cancer tissues are linked to worse outcomes for patients with hepatocellular carcinoma.

## Contribution

This study is the first to show that FAM96B acts as a tumor suppressor and predicts poor prognosis in hepatocellular carcinoma.

## Key findings

- FAM96B expression is significantly lower in hepatocellular carcinoma tissues compared to normal tissues.
- Low FAM96B levels correlate with larger tumors, advanced cancer stages, and worse survival rates.
- FAM96B inhibits liver cancer progression by inducing apoptosis and suppressing cancer cell growth.

## Abstract

Recently, studies on FAM96B functions mainly focused on its role in maintaining the normal physiological function of cells. However, the clinical implications of FAM96B in hepatocellular carcinoma (HCC) are still unclear.

FAM96B mRNA expression was detected in human HCC tissues and the matched nontumorous tissues by quantitative real-time reverse transcription (qRT-PCR) and then validated in The Cancer Genome Atlas (TCGA) database. Immunohistochemistry assay (IHC) was performed on all 137 cases of HCC samples to examine the protein level of FAM96B. Subsequently, the associations between FAM96B expression and clinicopathological parameters and prognosis were further analyzed.

The mRNA level of FAM96B was found to be significantly lower in HCC tissues compared to non-tumorous tissues, as observed in both the local hospital and TCGA database.Immunohistochemistry assay analysis revealed a decrease in FAM96B expression in 78 out of 137 cases, which was significantly associated with larger tumor size, higher Barcelona clinic liver cancer or Child stage, and early distant metastasis. Patients with low FAM96B levels tended to have an unfavorable disease-free and overall survival. Moreover, FAM96B was identified as an independent predictor of patient prognosis in both univariate and multivariate survival analyses. Mechanistically, FAM96B was found to inhibit cancer progression by inducing apoptosis in liver cancer cells and inhibiting their growth.

Our findings provide the first evidence suggesting the involvement of FAM96B in the progression of HCC. Additionally, FAM96B could potentially serve as a marker for tumor recurrence and prognosis in HCC patients.

## Linked entities

- **Genes:** CIAO2B (cytosolic iron-sulfur assembly component 2B) [NCBI Gene 51647]
- **Diseases:** hepatocellular carcinoma (MONDO:0007256), HCC (MONDO:0007256)

## Full-text entities

- **Genes:** CIAO2B (cytosolic iron-sulfur assembly component 2B) [NCBI Gene 51647] {aka CGI-128, CIA2B, FAM96B, MIP18}
- **Diseases:** Cancer (MESH:D009369), HCC (MESH:D006528), metastasis (MESH:D009362)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12001444/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12001444/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12001444/full.md

---
Source: https://tomesphere.com/paper/PMC12001444