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Clinicopathological Significance of Invasive Ductal Carcinoma with High Prevalence of CD44+/CD24-/low Tumor Cells in Breast Cancer

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¼ºÁö¿¬ ( Sung Ji-Youn ) 
°æÈñ´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç

±è±³¿µ ( Kim Gou-Young ) 
°æÈñ´ëÇб³ µ¿¼­½ÅÀÇÇк´¿ø º´¸®ÇаúÇб³½Ç
¹Ú¿ë±¸ ( Park Yong-Koo ) 
°æÈñ´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
ÀÌÁÖÈñ ( Lee Ju-Hie ) 
°æÈñ´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
±èÀ±È­ ( Kim Youn-Hwa ) 
°æÈñ´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
ÀÓ¼ºÁ÷ ( Lim Sung-Jig ) 
°æÈñ´ëÇб³ µ¿¼­½ÅÀÇÇк´¿ø º´¸®ÇаúÇб³½Ç

Abstract


Background: Epithelial tumor cells with a CD44+/CD24-/low immunoprofile may have the ability to cause breast cancer. We studied these cells and their clinicopathological significance.

Methods: The clinicopathologic findings of 100 invasive ductal carcinoma (IDC) cases and 45 ductal carcinoma in situ (DCIS) cases were reviewed. CD44+/CD24-/low tumor cells were identified by immunohistochemistry, and their clinicopathological implications in IDC and DCIS were analyzed.

Results: IDC with a high prevalence of CD44+/CD24-/low tumor cells was significantly associated with larger mass, higher grade, estrogen receptor (ER) negativity, and tumor cells with a higher frequency of metastasis. The proportion of CD44+/CD24-/low tumor cells in IDC, and its DCIS components was not significantly different, whereas the proportion of CD44+/CD24-/low tumor cells was higher in DCIS than in the DCIS component of IDC (p < 0.001).

Conclusions: IDC with a high prevalence of CD44+/CD24-/low tumor cells might correlate with aggressive features, such as ER and higher grades. Moreover, the proportion of CD44+/CD24-/low tumor cells in the DCIS components of IDC and DCIS might harbor different biology, which may lead to differences in cancer progression and early carcinogenesis.

Å°¿öµå

Neoplastic stem cells; CD44 protein; human; CD24 protein; human; Invasive ductal carcinoma; Carcinoma; intraductal; noninfiltrating

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