Splicing patterns of type XI collagen transcripts act as molecular markers for osteochondrogenic tumors.

Abstract

Primary transcripts for three distinct alpha chains of the type XI collagen molecule (alpha1(XI), alpha2(XI) and alpha3[XI]) undergo tissue-specific alternative splicing during the process of osteochondrogenesis. In the present study, we analyzed the splicing patterns of type XI collagen genes in osteochondrogenic tumors as well as in various normal tissues using the reverse transcription-polymerase chain reaction method. Analysis of normal subjects revealed the coordinated expression of short alpha1(XI), alpha2(XI) and alpha3(XI) transcripts in the normal differentiated cartilage. Osteochondroma followed this pattern, reflecting the highly chondrogenic phenotype of this benign tumor. Another benign tumor, chondroblastoma, exclusively expressed the long alpha1(XI) transcript, probably reflecting the lack of a chondrogenic nature. Among malignant chondrogenic tumors, the splicing patterns of type XI collagen transcripts were more complex, showing dissociated expression of long alpha1(XI) and short alpha2(XI) mRNAs. This expression pattern may reflect heterogeneous cell populations and may also reflect various levels of cell differentiation in malignant tumors. In addition, short alpha3(XI) expression switched to the long transcript as chondrosarcomas became more aggressive. Thus, the alternative splicing of type XI collagen genes seems to be oncodevelopmentally regulated and splicing analysis may therefore be a useful marker for chondrogenic tumors.

• Authors: Y Matsui, T Kimura, N Tsumaki, K Nakata, N Yasui, N Araki, N Hashimoto, A Uchida, T Ochi
• Journal: Cancer letters (Cancer Lett) Vol. 124 Issue 2 Pg. 143-8 (Feb 27 1998) ISSN: 0304-3835 [Print] Ireland
• PMID: 9500203 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Biomarkers, Tumor
• RNA, Messenger
• Collagen

Topics

• Alternative Splicing
• Biomarkers, Tumor (analysis)
• Bone Neoplasms (genetics, metabolism)
• Cartilage (metabolism)
• Chondroblastoma (genetics, metabolism)
• Collagen (biosynthesis)
• Humans
• Osteosarcoma (genetics, metabolism)
• Polymerase Chain Reaction
• RNA, Messenger (genetics, metabolism)
• Transcription, Genetic