Department of Oncogene Regulation, Chittaranjan National Cancer Institute, Kolkata, West Bengal, India.
Department of Surgical Oncology, Chittaranjan National Cancer Institute, Kolkata, West Bengal, India.
Mol Biol Rep. 2024 Jan 22;51(1):157. doi: 10.1007/s11033-023-08950-z.
This study aims to evaluate the role of cancer stem cell marker, CD44, and its ligand HA as potential molecular biomarker for early detection of HNSCC.
The expression profile (mRNA/Protein) of CD44 variants were analysed in primary HNSCC lesions and plasma of the patients. Then, prevalence of HA variants was analysed in plasma of the patients. The mRNA expression of CD44 variants, CD44S and CD44v3, were significantly high in both early (stage I/II) and late (stage III/IV) invasive lesions, with predominant expression of CD44v3 in the late-stage lesions. In plasma of HNSCC patients, increased levels of SolCD44, CD44-ICD and unique 62 KD CD44 variants with respect to standard CD44S were seen, in comparison to their prevalence in plasma of normal individuals. The abundance of CD44-ICD and 62 KD variants were significantly high in plasma of late stage HNSCC patients. Interestingly, significantly high level of low molecular weight HA(LMW HA) with respect to high molecular weight HA(HMW HA) was seen in plasma of HNSCC patients irrespective of clinical stages. On the contrary, high HMW HA level in plasma of normal individuals was seen. The high level of LMW HA in plasma of HNSCC patients might be due to combinatorial effect of increased mRNA expression of HA synthesizing enzyme HAS1/2/3 and HA degrading enzyme HYAL1/2, as seen in the primary HNSCC samples.
Thus, our data revealed the importance of specific CD44 and HA variants in plasma of HNSCC patients during its development as potential non-invasive molecular biomarker of the disease.
本研究旨在评估癌症干细胞标志物 CD44 及其配体 HA 作为早期检测头颈部鳞状细胞癌(HNSCC)的潜在分子生物标志物的作用。
分析了原发性 HNSCC 病变和患者血浆中 CD44 变体的表达谱(mRNA/蛋白)。然后,分析了患者血浆中 HA 变体的流行情况。在早期(I/II 期)和晚期(III/IV 期)侵袭性病变中,CD44 变体、CD44S 和 CD44v3 的 mRNA 表达均显著升高,晚期病变中 CD44v3 的表达更为明显。在 HNSCC 患者的血浆中,与正常个体相比,观察到 SolCD44、CD44-ICD 和独特的 62 KD CD44 变体相对于标准 CD44S 的水平升高,且 CD44-ICD 和 62 KD 变体的丰度在晚期 HNSCC 患者的血浆中显著升高。有趣的是,与正常个体相比,HNSCC 患者血浆中低分子量 HA(LMW HA)的水平显著升高,而高分子量 HA(HMW HA)的水平较低。相反,正常个体血浆中 HA 的水平较高。HNSCC 患者血浆中 LMW HA 水平升高可能是由于 HAS1/2/3 等 HA 合成酶和 HYAL1/2 等 HA 降解酶的 mRNA 表达增加所致。在原发性 HNSCC 样本中观察到了这一现象。
因此,我们的数据揭示了特定的 CD44 和 HA 变体在 HNSCC 患者发展过程中在血浆中的重要性,它们可能成为该疾病的潜在非侵入性分子生物标志物。