# P16 and CD44 as Biomarkers for Predicting the Progression of Immature Polypoid Squamous Metaplasia of the Cervix

**Authors:** Tamar Svanadze, Teona Turashvili, Shota Kepuladze, George Burkadze

PMC · DOI: 10.7759/cureus.81661 · Cureus · 2025-04-03

## TL;DR

This study identifies P16 and CD44 as potential biomarkers to predict the progression of immature polypoid squamous metaplasia to cervical intraepithelial neoplasia.

## Contribution

The study demonstrates that P16 and CD44 are highly predictive of IPM progression to high-grade CIN.

## Key findings

- Higher P16 and CD44 expression levels are significantly associated with higher-grade CIN lesions.
- P16 had 100% positive predictive value for IPM progression to CIN2 or CIN3.
- CD44 had 90% positive predictive value for IPM progression to CIN.

## Abstract

Cervical intraepithelial neoplasia (CIN) is a well-established precursor of cervical cancer, while immature polypoid squamous metaplasia (IPM) has been hypothesized as a possible early lesion in cervical carcinogenesis. However, the mechanisms underlying IPM progression to CIN remain unclear. Therefore, identifying reliable biomarkers to predict progression is crucial. This study evaluates the immunohistochemical expression of P16, CD44, estrogen receptor (ER), and progesterone receptor (PR) in CIN and IPM, focusing on their prognostic significance in IPM-to-CIN progression.

A total of 227 cervical tissue samples were analyzed, including CIN1 (N=30), CIN2 (N=30), CIN3 (N=32), IPM (N=60), mature squamous metaplasia (N=45), and reactive ectocervix - control (N=30). P16, CD44, ER, and PR expression were assessed immunohistochemically. Additionally, clinical HPV (human papillomavirus) status was determined via PCR, and marker expression was correlated with lesion grade using a standardized study algorithm. A subgroup of 40 IPM cases that progressed to CIN was analyzed to identify possible markers predictive of progression.

Our results demonstrate that higher P16 and CD44 expression levels are significantly associated with higher-grade CIN lesions (p < 0.001). P16 and CD44 expression also strongly predicted IPM progression: P16 showed a 100% positive predictive value (PPV) for progression to CIN2 or CIN3, meaning all IPM cases with moderate or strong P16 expression advanced to high-grade CIN. CD44 had a 90% PPV for CIN progression, suggesting a strong correlation with aggressive epithelial transformation.

Although ER and PR expressions were statistically significant (p < 0.05), they were not predictive markers of CIN progression. These findings highlight P16 and CD44 as possible biomarkers for identifying high-risk IPM lesions and assessing the likelihood of progression to CIN2/3.

## Linked entities

- **Genes:** CDKN2A (cyclin dependent kinase inhibitor 2A) [NCBI Gene 1029], CD44 (CD44 molecule (IN blood group)) [NCBI Gene 960], EREG (epiregulin) [NCBI Gene 2069], PGR (progesterone receptor) [NCBI Gene 5241]
- **Diseases:** cervical intraepithelial neoplasia (MONDO:0022394), cervical cancer (MONDO:0002974)

## Full-text entities

- **Genes:** PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, CDKN2A (cyclin dependent kinase inhibitor 2A) [NCBI Gene 1029] {aka ARF, CAI2, CDK4I, CDKN2, CMM2, INK4}, CD44 (CD44 molecule (IN blood group)) [NCBI Gene 960] {aka CDW44, CSPG8, ECM-III, ECMR-III, H-CAM, HCELL}
- **Diseases:** Polypoid Squamous Metaplasia of the Cervix (MESH:D065309), CIN2/3 (MESH:C537153), cervical carcinogenesis (MESH:D063646), CIN (MESH:D002578), cervical cancer (MESH:D002583), squamous (MESH:D002294)
- **Species:** Human papillomavirus (species) [taxon 10566]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12049178/full.md

## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC12049178/full.md

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Source: https://tomesphere.com/paper/PMC12049178