Gaffoor Nidha, Krishnamurthy Jayashree
Department of Pathology, Dr. Chandramma Dayananda Sagar Institution of Medical Education and Research, Ramanagara, Karnataka, India.
Department of Pathology, JSS Medical College, Mysuru, Karnataka, India.
J Lab Physicians. 2023 Feb 24;15(3):354-360. doi: 10.1055/s-0043-1761925. eCollection 2023 Sep.
Breast cancer is an epithelial malignancy; however, stroma plays a key role with its stimulatory and inhibitory factors in modulating tumor invasion and metastasis. CD10, a matrix metalloproteinase, is known to regulate cell adhesion, migration and helps in determining the progression of tumor. This knowledge helps to identify specific signals that promote growth, dedifferentiation, invasion, metastasis and serve as target for better therapeutic management. The aim of this study was to estimate frequency of expression of stromal CD10 and assess its prognostic significance in breast carcinomas by correlating with known prognostic factors. Morphological parameters of 62 cases of carcinoma breast were studied on H&E (hematoxylin and eosin) stained sections and expressions of estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2/neu), and CD10 on manually constructed tissue microarray sections by immunohistochemistry (IHC). Staining pattern, percentage of stained cells, and intensity of stains were evaluated and IHC scoring of all markers was done. CD10 scores were correlated with the known prognostic factors (ER, PR, and HER2/neu). A -value less than 0.05 was considered as significant. Stromal expression of CD10 was found in 82.3% of cases and it was significantly associated with increasing tumor size ( = 0.012), increasing tumor grade ( = 0.001), lymph node metastasis ( = 0.018), necrosis ( = 0.008), lymphovascular invasion ( = 0.008), ER negativity ( = 0.001), PR negativity( = 0.007), HER 2 positivity ( = 0.012), triple-negative molecular subtypes ( = 0.001), and poor prognostic groups ( = 0.01). CD10 can be used as an independent prognostic stromal marker and this will help to envisage new therapeutic strategies.
乳腺癌是一种上皮性恶性肿瘤;然而,基质通过其刺激和抑制因子在调节肿瘤侵袭和转移中发挥关键作用。CD10是一种基质金属蛋白酶,已知其可调节细胞黏附、迁移,并有助于确定肿瘤的进展。这一认识有助于识别促进肿瘤生长、去分化、侵袭和转移的特定信号,并作为更好的治疗管理靶点。本研究的目的是通过与已知预后因素相关联,评估基质CD10的表达频率,并评估其在乳腺癌中的预后意义。对62例乳腺癌病例的苏木精和伊红(H&E)染色切片进行形态学参数研究,并通过免疫组织化学(IHC)在手工构建的组织微阵列切片上检测雌激素受体(ER)、孕激素受体(PR)、人表皮生长因子受体2(HER2/neu)和CD10的表达。评估染色模式、染色细胞百分比和染色强度,并对所有标志物进行IHC评分。将CD10评分与已知预后因素(ER、PR和HER2/neu)相关联。P值小于0.05被认为具有统计学意义。在82.3%的病例中发现有基质CD10表达,且其与肿瘤大小增加(P = 0.012)、肿瘤分级增加(P = 0.001)、淋巴结转移(P = 0.018)、坏死(P = 0.008)、淋巴管浸润(P = 0.008)、ER阴性(P = 0.001)、PR阴性(P = 0.007)、HER2阳性(P = 0.012)、三阴性分子亚型(P = 0.001)和预后不良组(P = 0.01)显著相关。CD10可作为一种独立的预后基质标志物,这将有助于设想新的治疗策略。