Table 2.
Molecular markers studied in thyroid FNAC aspirates and thyroid cancer specimens from India
| Authors | Number of samples | Molecular marker studied | Test performance |
|---|---|---|---|
| Aron et al., Delhi [26] | 70 | Galectin-3 | The smears stained positive for Galectin-3 in 80% of PTCs, 37.5% of FNs, and in 60% of benign nodules. |
| Choudhury et al., Delhi [27] | 25 | p53 and Ki-67 | Ki-67 scores ranged from 2.2 to 13 in the DTCs while ranged 0.5–2 in benign nodules |
| Mehrotra et al., Lucknow [28] | 123 | Ki-67 and AgNORs | Mean AgNOR counts and Ki-67 labelling index were consistently higher in Follicular cancers compared to adenomas and hyper plastic nodules |
| Hemalatha et al., Vellore [29] | 277 | BRAF V600E | 27.2% of FNA samples were positive for mutations; only 1 sample of those labelled as AUS was positive for BRAF; BRAF positive PTCs had higher rates of lymph node metastasis |
| George N et al., Lucknow [30] | 109* PTC | BRAF V600E, RAS, RET/PTC | BRAF V600E noted in 51.38%, NRAS in 7.34% of all PTCs. No RET/PTC rearrangements were observed |
| Ahmad F et al., Mumbai [31] | 95* Thyroid tumours | BRAF V600E | 38% were BRAF positive |
| George N et al., Lucknow [32] | 30* FVPTC | BRAF and RAS and NIS expression | BRAF mutation was observed in 62.5%; No NRAS mutation was found. Sodium iodide symporter (NIS) expressions were down-regulated in invasive and infiltrative/diffuse FVPTC but not in NIFTP. |
| Krishnamurthy A et al., Chennai [33] | 79* DTC | BRAF V600E | 31% of the DTCs were positive for BRAF |
| Nair CG et al., Kochi [34] | 59* PTC | BRAF V600E | 51% harboured BRAF V600E mutation, but the mutation status was not associated with aggressive tumour factors and adverse outcome. |
| Chakraborty A et al., Mumbai [35] | 140* Thyroid tumours | BRAF V600E | BRAF V600E in 53.4% of PTC. Classic PTC (61%) FVPTC (11.7%). Significant correlation between BRAF mutation status and extra-thyroidal invasion, lymph node metastasis, and tumour stage. |
*Studies on thyroid cancer specimens